BioMed Research International

BioMed Research International / 2016 / Article

Review Article | Open Access

Volume 2016 |Article ID 5062064 |

Johnny E. Moore, Davide Schiroli, C. B. Tara Moore, "Potential Effects of Corneal Cross-Linking upon the Limbus", BioMed Research International, vol. 2016, Article ID 5062064, 11 pages, 2016.

Potential Effects of Corneal Cross-Linking upon the Limbus

Academic Editor: Ciro Costagliola
Received03 Apr 2016
Accepted10 Jul 2016
Published05 Sep 2016


Corneal cross-linking is nowadays the most used strategy for the treatment of keratoconus and recently it has been exploited for an increasing number of different corneal pathologies, from other ectatic disorders to keratitis. The safety of this technique has been widely assessed, but clinical complications still occur. The potential effects of cross-linking treatment upon the limbus are incompletely understood; it is important therefore to investigate the effect of UV exposure upon the limbal niche, particularly as UV is known to be mutagenic to cellular DNA and the limbus is where ocular surface tumors can develop. The risk of early induction of ocular surface cancer is undoubtedly rare and has to date not been published other than in one case after cross-linking. Nevertheless it is important to further assess, understand, and reduce where possible any potential risk. The aim of this review is to summarize all the reported cases of a pathological consequence for the limbal cells, possibly induced by cross-linking UV exposure, the studies done in vitro or ex vivo, the theoretical bases for the risks due to UV exposure, and which aspects of the clinical treatment may produce higher risk, along with what possible mechanisms could be utilized to protect the limbus and the delicate stem cells present within it.

1. Clinical Applications of CXL

In the last decade corneal cross-linking (CXL) has become the routine treatment for progressive ectasias including keratoconus (KC) and Pellucid Marginal Degeneration (PMD) [1, 2]. This approach exploits the combined properties of ultraviolet A (UVA, 315–400 nm) and riboflavin: UV irradiation excites the fluorescent molecule to a triplet state, with consequent generation of a singlet oxygen and superoxide radical. These radical products are then able to strengthen the corneal stroma and also possibly more importantly increase the stromal resistance to enzymatic degeneration [3] forming covalent bonds in the collagen.

This process is also cytotoxic, as planar molecule riboflavin intercalates between the bases of DNA and RNA and, once activated, it is able to oxidate the nucleic acids [46]. Thanks to this characteristic CXL has been used in transfusion medicine to diminish the risk of transfer of infectious agents [7] and more recently has become a recognized technique as a possible adjunctive or primary treatment for infectious keratitis [8, 9]. Moreover cross-linking is able not only to kill infective organisms within the corneal stroma but also to arrest the corneal melting process caused by the release of proteolytic enzymes by both microbes and invading protective white blood cells [1012].

2. Commercial CXL

Several alternative methods to perform CXL have been developed as summarized in various literature reviews [13]. The advantages and disadvantages of the different techniques in terms of the limbal safety are discussed later in this review.

2.1. Standard Epithelium-Off CXL

In the standard CXL the central part of the cornea (8-9 mm) of the cornea is irradiated with UVA at 3 mW/cm2 for 30 min. The corneal thickness has to be checked in the pre-CXL procedure and has to be greater than 400 μm, to avoid damage to the endothelium. To enable the complete penetration of the riboflavin in the stroma the epithelium is debrided. Topical antibiotics and corticosteroids are prescribed after the procedure until corneal reepithelialisation.

2.2. Accelerated CXL

Accelerated CXL protocols exploit UVA energies with higher fluencies and shorter exposure times. In this way, following the Bunsen-Roscoe law of reciprocity, the endothelial UVA dosage can be kept constant, below the cytotoxic threshold, but with the same efficiency. This is potentially an advantage for patient safety, as the time in which the keratocytes are exposed to UVA is reduced, with probably a decreased rate of damage and apoptosis. Some clinical studies have demonstrated the effectiveness of this technique and more studies are currently ongoing.

2.3. Epithelium-On (Epi-On) CXL

Epithelial debridement is necessary to allow stromal diffusion of riboflavin: as confirmed by several studies riboflavin hydrophilic nature stops it from penetrating the tight junctions of the intact epithelial barrier.

The development of an epi-on CXL is however desirable to reduce risks of keratitis and of other possible complications. For this reason several alternative solutions have been developed; between them the most ones promising are some novel formulations of riboflavin, which facilitate the transepithelial absorption, and iontophoresis [13, 29]. This last option in particular is giving encouraging results also in clinical studies, as it is discussed in the epi-on chapter. The nature of the small riboflavin molecule which is negatively charged at physiological pH and soluble in water makes it highly suitable for iontophoretic transfer.

3. Clinical Complications of CXL

The results from an increasing number of long-term studies have recurrently demonstrated that this is a safe method but there are also various different complications observed after CXL treatments [30, 31], as summarized in Table 1. One major problem is the increased risk of infective keratitis due to delayed reepithelialisation, [14, 15, 18, 32, 33] along also with cases of sterile peripheral corneal infiltrates [34]. The incidence of infective keratitis, as indicated from these published cases, would appear to be significantly higher than that reported in a very similar procedure called photorefractive keratectomy (PRK) [35]. IN PRK an identical 9 mm diameter epithelial defect is created in the cornea prior to treatment of the corneal stroma with a short UV wavelength 193 nm excimer laser, while in CXL a longer UVA wavelength (360 nm) is utilized for a much longer period of time.


Bacterial keratitis[1416]Various organisms have been implicated with most commonly found to be of staphylococcal variant.
The corneal epithelium is removed during the CXL treatment (epithelium-off method) to permit the diffusion of the riboflavin into the corneal stroma [17]. This step however reduces the immune-protective function of the superficial corneal layer against infectious agents [18].
Many surgeons are now forgoing the use of lenses postoperatively and increasing the frequency of antimicrobial drops to further reduce the risk of microbial infection after CXL [19]. Moreover linear abrasions can reduce the healing time and a CXL without removing the epithelium can be used [17, 18].
Acanthamoeba keratitisAcanthamoeba keratitis is facilitated by the removal of the epithelium particularly if a CLenses is left in place.

Herpes reactivation[20]It is well recognized that UV light can cause reactivation of herpes. This commonly occurs with those travelling to sunny climates or skiing in the winter.Prophylactic systemic antiviral treatment in patients with history of herpetic disease.

Oedema[21, 22]Can be permanently caused by damage to the endothelial cells.70% of CXL treated eyes show mild stromal oedema. Some significant cases were reported; however all of them resolved.

Haze[23, 24]In most of the cases it is temporary; only in 8-9% it was reported to last for long.

Sterile infiltratesUV treatment alters the response to antigens. Reported in 7-8% of the cases, it can be treated with topical steroid.

Endothelial damage[21, 22, 25, 26]It happens in the case of a stromal thickness less than 400 μm or incorrect focusing. The threshold level of irradiance which could cause damage to the endothelium was found to be 0.35 mW/cm2, but this level is easily avoided if the corneal depth of 400 m is used as a cutoff level, with irradiance falling to 0.18 mW/cm2 when using the standard protocol. To date longer-term studies of corneal cross-linking have not shown any increased loss of endothelial cells after cross-linking compared to either the normal eyes or post-LASIK eyes [27, 28].

Treatment failure7.6% of keratoconic progression following treatment at one-year followup [19].

In response to the increase in infective keratitis, which may result from a localized alteration in corneal immune status, clinicians have modified their postoperative treatment advice often dispensing with the use of CLenses and increasing the frequency of antibiotic usage (unpublished data).

Epithelial-on (epi-on) CXL further decreases the possibility of contracting keratitis, as in this case the important epithelial barrier is kept intact [2]. Recent advances in the epi-on CXL, like iontophoresis and transepithelial CXL [36, 37], improve the transfer of riboflavin facilitating deep stromal penetration, making the epi-on CXL a potentially safer alternative to the standard epi-off CXL with comparable clinical outcomes.

In parallel with the risk of keratitis a major concern is the possibility of inducing toxicity or cell death to the endothelium, keratocyte, and limbal cells. The risk of damaging the endothelium appears to be minimal if certain stromal thickness levels are maintained prior to treatment. Oxygen free radicals and superoxide radicals, however, cause significant keratocyte toxicity and death [17, 38]. This cellular toxicity is however limited to the anterior 300 μm with a toxic cellular threshold of 0.5 mW/cm2 for 30 mins of treatment. Possible damage to the endothelium could be a problem as it lacks regenerative capacity, but cell density, morphology, and cell count were demonstrated to be unaltered as long as the criteria of maintaining 400 μm of minimum stromal depth, which ensured sufficient absorption of UVA exposure to prevent attainment of the toxic threshold of 0.35 mW/cm2 from a 30 min exposure [3]. Moreover riboflavin itself has the role of photosensitizer but it also absorbs the UVA radiation furtherly protecting the endothelium, so for a thin stroma it might be possible to increase the amount of riboflavin for improving the UVA protection through the stroma [29].

An interesting matter of debate is instead the toxic threshold for possible UVA/riboflavin induced oxidative damage to the permanent epithelial and/or anterior stromal stem cells of the eye contained in the limbal niche, about which there are only a few reported studies.

4. UV-Induced Mechanisms of Damage

UVA has effect on various cellular chromophores, like flavins and amino acids (e.g., tryptophan, tyrosine, and histidine). Reactive oxygen species (ROS: superoxide anion and the hydroxyl radical ), as well as nonradicals like hydrogen peroxide (H2O2 and ) are then generated by these molecules after the UV absorption.

Mammalian cells have developed two main systems to protect themselves from the ROS oxidative stress, which represents the major cause of risk and the initial step for the developing of an UV-induced skin cancer.

The first mechanism of protection is the nonenzymatic antioxidants, α-tocopherol, ascorbic acid, glutathione, and β-carotenoids, while the other one is constituted by the enzymatic antioxidants such as superoxide dismutase (SOD), catalase, and glutathione peroxidase (GPx) [39].

UVA irradiation induces cyclobutane pyrimidine dimers (CPDs) in DNA, while both UVA and UVB can promote the formation of oxidized DNA, like 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxo-dG).

This is the most frequent UVA-induced oxidative base lesion and it can cause the G to T transversions. 57% of the mutations occurring after UVA treatment have been reported in fact at the TT sites (with C, CT, or CC sites at 18, 11, and 14%, resp.) [40].

In human squamous cell tumors the G-T transversions are more common than the C-T, showing a specific fingerprint mutations that strongly associate the UVA-induced DNA damage to human skin carcinogenesis [41].

Several in vitro experiments have been reported to characterize the amount and the spectra of the possible lesion and mutation, but these are quite variable, depending on the actual experimental conditions, and, due to the low mutagenic potential of UVA, it is quite difficult to quantify the ratio between the mutation induction and the UV dosage [42].

Despite these difficulties most of the studies seem to be in accordance with the fact that UVA induces a higher number of delayed mutations with respect to UVB and X-radiation although only few immediate mutations are produced [4346].

5. Consequences of UV Exposure on Ocular Surface and Limbus

5.1. UV Ocular Surface Exposure Diseases

A wide range of different pathologies have been associated with UV exposure and they can affect different parts of the eye, including cataract and retinal macular degeneration. UV exposure has been further implicated in several diseases involving the conjunctiva and cornea like pterygium and pinguecula, photokeratitis, keratopathy, and ocular surface squamous neoplasia [47].

5.2. UV Exposure and Eye Cancer

It is well accepted that UV plays a major role as a mutagen in different pathologies, firstly cutaneous cancer [42]. It is similarly well established that the occurrence of cancers is related to sun exposure and hence skin cancers are more common in nontanning individuals, areas of the body with the highest sun exposure (face, ears, and backs of hands), and regions with high levels of UV exposure [48].

Ocular surface cancers are quite rare in the general population, testifying to the ability of the innate system to manage UV-induced cellular changes on this surface, but it is also true that the incidence is much higher in countries such as Australia, where there are high numbers of Caucasians. These lesions seem to focus anatomically around the limbal region in keeping with the presence of long-lived stem cells in that region.

Usually in short-lived cells a mutation does not tend to represent a problem because it disappears with cell death, but it can represent a serious problem in long-lived cell such as the limbal stem cells. They potentially survive for the whole life of the individual and hence the propensity to accumulate oncogenic damage over time makes it more likely to result in invasive cancer. As the epithelial stem cells in the cornea are specifically retained at the peripheral limbal region this is in keeping with the high incidence of ocular surface cancer found to be present in this region [48].

5.3. The Role of the Limbus

The limbal region, situated at the anterior portion of the cornea, hosts the stem cells involved in the corneal epithelium turnover. Their role in maintaining the health of the corneal epithelium over a lifetime is fundamental for the correct functioning of the cornea and deficiency or loss of these cells is associated with a characteristic phenotype of the ocular surface consisting of an irregular epithelium, with conjunctival epithelial ingrowth, vascularization, goblet cells, recurrent epithelial breakdown, and chronic surface inflammation [49, 50].

These limbal stem cells are attached to the basement membrane and deep within the valleys of an undulated region of stroma called the palisades of Vogt [51, 52]. They are usually maximally concentrated in the superior region of the limbus normally protected by the upper lid and in the inferior limbus, the area protected by the lower lid [53]. The vascularization and pigmentation of this area are thought to take also part in the physical defense of the stem cells from UV exposure [54, 55]. Similarly to what happens in the skin sporadic melanocytes were in fact founded in the palisades of Vogt, they have dendritic processes surrounding the basal limbus epithelial cells expressing K19 (+), and they form a melanin unit that protects the limbus from the UV. Melanin has in fact antioxidative properties and it might hence protect from the UV-induced oxidant formation in the cornea epithelium [56].

Moreover recent studies have also defined a stromal keratocyte stem cell pool within the anterior stroma also underneath and adjacent to the epithelial palisades of Vogt [48] (Figures 1 and 2).

6. CXL: UV Damage of the Limbal Cells

6.1. The UV Damage of the Limbus after CXL Treatment

As outlined earlier, CXL induces cytotoxicity and keratocyte cell death [5759], but generally this does not seem to affect the subsequent clinical epithelial surface once reepithelialisation has occurred.

During the process of clinical CXL the superior and inferior limbal region, which are shown to have maximum stem cells and which are normally hidden by the upper and lower lids [53], are now no longer protected from the prolonged iatrogenic UVA exposure. It is a worry to clinicians as to whether mutagenic changes could be induced within the corneal limbal stem cells during this treatment and any ensuing problems may not show themselves until much later in life.

Though during CXL the limbus of the eye is not deliberately treated, however, it is very difficult, without using a regional anesthetic block to cause extraocular muscle paresis, to adequately protect the limbus from UV exposure during the procedure (Figure 1).

This risk is also higher in the cases of treatment of pellucid marginal corneal degeneration (PMD), where the irradiated area is often peripheral and close to the limbus [60]. The removal of the central epithelium increases the amount of riboflavin transferred into the peripheral cornea and limbal region, greatly enhancing the oxidative effect upon cells affected by UVA within that region. During the deepithelialisation further changes, such as a slough of some of the overlying layers, actually at the limbal region, of epithelium can occur. These layers normally absorb 20% of the UVA passing through the cornea [29, 61]. This will again remove some further aspects of the normal protective anatomical barriers from UVA damage we previously outlined regarding the position of the corneal stem cells located in two niches (the palisades of Vogt and the epithelial crypts). Melanin within the basal region of the limbal epithelia normally acts as a further shield and protector against irradiation. This is supported by the fact that Wollensak and collaborators found viable keratocytes in the deeper layers of the cornea after riboflavin-UVA [62]. However all this resident protection which functions exceptionally well in normal life may not be sufficient to adequately guarantee the safety of the limbal niche within the altered clinical situation of corneal CXL [63].

Several studies have now focused upon this issue, suggesting the potential damaging effect of CXL treatment upon the limbus with the consequent risk of subsequent morbidity for the patients, particularly of developing ocular surface cancer, later in life.

Many publications report studies which demonstrate the risk of potential iatrogenic limbal damage.

The expression of proapoptotic genes was shown to be induced by CXL in an in vitro study [63]. Moreover CXL seems to inhibit the regeneration of cultured human limbal epithelial cells [62] and of cells extracted from cadaver eyes previously treated with CXL [64].

Ex vivo (corneas from donor) analysis confirm these results, showing the UV damage to the limbal epithelial cells through the measurement of DNA damage markers and oxidative damage of nuclear DNA [65], while in a recent case study a patient treated by CXL has developed a conjunctival intraepithelial neoplasia (the preliminary stage of invasive squamous cell carcinoma) [66]. This last publication represents to date the only in vivo reported case demonstrating such a deleterious effect of CXL upon the limbus as the other in vivo study [38], done on rabbit eyes, did not demonstrate a pathological effect upon the limbus.

A study on the incidence of the AA-TT mutation caused by the UVA exposure mutations on the DNA of treated cells or tissues might be useful to further confirm the damaging role of the UVA on the limbal cells, as described for the UVA fingerprints analysis in skin cancer [67].

Given the significant potential risk of damage to the limbus it is advisable to exclude from CXL treatment any subjects where there is further comorbidity which could increase the likelihood of induced limbal stem cell problems. This is the case where there is preexisting underlying limbal stem cell deficiency (LSCD) or xeroderma pigmentosum.

7. How to Reduce the Limbus Exposure

The before mentioned issues raise several questions: are there better ways by which the limbal region containing stem cells could be protected during the CXL procedure? Could CXL particularly for the limbal region be achieved in any other nontoxic fashion without the use of UVA?

7.1. Physical Protection

Usage of polymethyl methacrylate rings, Vidaurri rings, or other rings with UV blockers can prevent CXL-induced limbal stem cells damage [38]. These physical blocking methods seem to provide only partial protection of the limbus with only 20% of the epithelial stem cells coming from treated cadaver that maintains the stemness [68]; one of the main problems in effective protection using this methodology is the constant ocular movement. Other researchers recently proposed the utilization of 8.5 mm punched UV-block contact lenses during CXL [69].

7.2. Accelerated Corneal Cross-Linking

A recent study that compared the accelerated corneal collagen cross-linking (ACXL) with the normal CXL on ex vivo-cultured limbal epithelial cells proved that the first one is safe [7072]. This procedure utilizes an increased intensity of UV exposure in parallel with a decreased duration (in the standard CXL the intensity is 3 mW/cm2 and the duration is 30 min, while in ACXL these parameters can vary between 30 mW/cm2 for 3 min, 18 mW/cm2 for 5 min, and 9 mW/cm2 for 10 min. More recently an ultrafast version has been released to the market providing an irradiance intensity of 43 mW/cm2 [36]) with the total amount of delivered energy that does not change between the two treatments [7375]. The effective ability of the accelerated CXL in producing the same results to classical CXL is still a matter of debate, with several contrasting results [76]; however quite recently Cheng and collaborators showed how the conventional method still seems to have a better clinical outcome, with greater corneal flattening and reduction in mean keratometry. The demarcation line was also shown to be deeper in conventional CXL [77].

This comparison demonstrates that the accelerated technique still needs further improvement prior to acceptance within the clinic. Moreover, despite the fact that several comparative clinical studies have been conducted [2], there is not as yet an accepted unique protocol for ACXL and large clinical trials are needed.

7.3. Chemically Accelerated Cross-Linking

CXL might be accelerated using different compounds alternative to riboflavin or along with it. Vitamin-E was for example proven to enhance the riboflavin solution, shortening the time of exposure, as confirmed in a clinical study with 19 patients. In this case the UVA was irradiated for 2 times, 5 min. at 3 mW/cm2 each, with final results comparable to the one of the canonical CXL [78, 79].

7.4. UV Devices

It is possible to direct the treatment in a delimited area using some of the specific devices for UV irradiation. An area of 8 mm in diameter, which can be selected in all the modern CXL devices (Table 2), should avoid UV to the limbus, the sclera, or the goblet cells; however even using an 8 mm irradiating device, eye movement makes it almost impossible to avoid limbal irradiation. One of the current modern devices called UV-X utilizes a special radiation homogenizer, to prevent endothelial damage by preventing local radiation spikes [17]. More studies are necessary however to confirm that this treatment is beneficial in also preventing damage to the limbus and particularly the limbal basal epithelial cells.

UV deviceProcedureIrradianceSpot sizes

XLink (Optos, Dunfermline, UK)Standard 30 min CXL0.5–5 mW/cm26, 8, and 10 mm

CBM Vega XLink Cross-Linking System (Carleton Optical, Chesham, UK)Standard 30-min CXL3 mW/cm24 to 11 mm

The LightLink CXL (LightMed, San Clemente, Calif., USA)From 3 to 30 min length protocolsBetween 0.5 and 30 mW/cm24 to 11 mm

The UV-X 2000 Cross-Linking System (IROC Innocross, Zurich, Switzerland)Used for in a 10 min accelerated CXL procedure12 mW/cm27.5 mm, 9.5 mm

KXL System (Avedro, Waltham, Mass., USA)Used in ultrafast accelerated CXL (<3 min of UVA exposure). It gave a positive outcome only in a small number of KC patients and in combination with the LASEK procedureIntensity of 30 mW/cm2Up to 11 mm

7.5. Antioxidant Treatment

UVA-induced mutations have been demonstrated to occur long after the initial exposure [43]. Various intracellular enzymes are induced in response to UVA light induced oxidative stress and reactive oxygen species (ROS); these include superoxide dismutase (SOD), catalase, and glutathione peroxidase (GPx) [39]. This has led to various attempts to counteract oxidative damage through the use of nonenzymatic antioxidants [80].

During CXl however, it would be counterproductive to try to utilize such methodology, as this could block the actual desired effect of the treatment which utilizes the oxidative stress to induce cross-linking and therapeutic effect. A potential way to protect the limbal stem cells while still achieving the desired oxidative induced effect would be to assess the possibility of upregulation of an intracellular protective response against ROS. Examples of this type of approach might include single or repetitive very low-dose UVA to attempt to upregulate the various antioxidant intracellular enzymes such as manganese superoxide dismutase (MnSOD) or glutathione peroxidase (GPx) [39, 81]. Similar strategies have been used in other forms of medicine using ischaemic reperfusion models where pretreatment with low-dose recurrent ischaemia protects against subsequent oxidative damage [82].

7.6. Epithelium-On (Epi-On) Cross-Linking

CXL can be performed while avoiding removal of the epithelium; several studies and reviews analyze this interesting new area of research. The main techniques use either epithelial tight junction disruptors or iontophoresis [76, 83]. Iontophoresis (I-CXL) in particular seems to be the most promising technique to enhance the delivery of riboflavin in an epi-on CXL, even if still not providing the same level of efficacy as classical CXL is currently the most promising transepithelial technique [29, 36]: The riboflavin penetration into the corneal stroma as well as the corneal rigidity was found ex vivo to be comparable to that obtained with standard CXL [37, 84]. Moreover another study showed low toxicity from I-CXL, even if the results of the concentration of riboflavin in the corneal stroma in this case were less as demonstrated by HPLC, found 2-fold less concentrated with respect to standard epi-on CXL [85]. However the mechanical strength of the cornea measured in the transepithelial I-CXL was shown to be comparable to the one measured with the standard procedure [86]. Clinical results published for I-CXL with a short 15-month followup show I-CXL to be equally effective at stopping the progression of keratoconus and improving keratometric and visual parameters. long-term clinical outcomes however have still not been investigated [8790]. Various other epithelium-on techniques, which exploit different formulations of riboflavin with an increased stromal absorbance, show inconsistent results: in a randomized clinical trial with one of the commercial protocols showing keratoconus still progressing 1 year after treatment in 23% of the cases [91]; and this seemed to be confirmed by in vitro studies on the available commercial protocols [87] and by other preliminary clinical studies [87]. Opposite results however have been reported by a couple of other clinical studies [92, 93], with positive outcomes demonstrated up to 18 months after the treatment. Further clinical and in vitro studies are therefore necessary to assess the status of the current available protocols while, in parallel, it is desirable that research continues upon novel formulations able to increase the bioavailability of riboflavin within the stroma. It is known that the epithelium absorbs about 20% of UVA radiation; therefore clinicians and researchers need to take this into account if they want to deliver enough energy to the stroma while keeping this below the endothelial toxicity threshold [29].

Despite the research that still needs to be done, epi-on procedures are very promising, as they can be applied to patients with a corneal thickness below 400 μm [94]; they can also reduce postoperative pain and similarly the risk of infective keratitis and improve the healing time.

8. Future Research: Alternatives to CXL

Many alternative photochemical as well as chemical [95] CXl methods are currently under research [2].

Photosynthetic pigments (chlorophylls and bacteriochlorophylls) that produce and radicals, with the consequent protein cross-linking, have been tested in rabbit cornea, giving a significant stiffening in vivo and ex vivo, after excitation with a near-infrared illumination [96]. The authors of this study found less adverse effects in the near-IR than after UVA exposure, but the toxicity levels of near-IR illumination on the eye need further evaluation [97].

In another study the Rose Bengal dye was excited by green light and led to an increased corneal stiffness, without toxicity to keratocytes [98].

Moreover in vitro studies suggest the possibility of substitution of UVA excitation of the riboflavin with one utilizing instead a femtosecond laser [12].

Using chemical CXL we can list various different methods that do not need any irradiance.

Most of the chemical cross-linkers however are toxic and cannot be used in vivo (e.g., formaldehyde and glutaraldehyde).

However to use β-nitroalcohols has been proposed, chemical molecules having a cross-linking mechanism similar to that of formaldehyde. Though they have never been tested for this purpose, we know from their numerous industrial applications that they have a positive safety record; for this reason they could be studied for use in CXL applications [99, 100]. Glyceraldehyde has been proven to function as a collagen cross-linker in a rabbit bullous keratopathy model [101].

Moreover a recent study also demonstrated that genipin (an active molecule derived from the plant Gardenia jasminoides) is also able to produce a CXL effect similar to CXL in porcine eyes, with minimal endothelial toxicity [102, 103].

9. Conclusions

CXL has revolutionized the management of these difficult progressive conditions such as KC and PMD, changing the clinical landscape from one of patiently watching a cornea degenerating without any ability to prevent the potential eventual requirement of a corneal graft. Instead there is a new arena whereby young people can be prevented from going down that intractable route of increasing morbidity and enabled instead to continue with their pastimes and other contact sports activities. It is therefore imperative that we continue to research this topic to ensure that this radical new therapy has long-term safety.

Competing Interests

The authors declare that they have no competing interests.


  1. F. Raiskup, A. Theuring, L. E. Pillunat, and E. Spoerl, “Corneal collagen crosslinking with riboflavin and ultraviolet-a light in progressive keratoconus: ten-year results,” Journal of Cataract and Refractive Surgery, vol. 41, no. 1, pp. 41–46, 2015. View at: Publisher Site | Google Scholar
  2. N. Sorkin and D. Varssano, “Corneal collagen crosslinking: a systematic review,” Ophthalmologica, vol. 232, no. 1, pp. 10–27, 2014. View at: Publisher Site | Google Scholar
  3. E. Spoerl, M. Mrochen, D. Sliney, S. Trokel, and T. Seiler, “Safety of UVA-riboflavin cross-linking of the cornea,” Cornea, vol. 26, no. 4, pp. 385–389, 2007. View at: Publisher Site | Google Scholar
  4. V. Kumar, O. Lockerble, S. D. Kell et al., “Riboflavin and UVlight based pathogen reduction: extent and consequence of DNA damage at the molecular level,” Photochemistry and Photobiology, vol. 80, pp. 15–21, 2004. View at: Google Scholar
  5. A. Tsugita, Y. Okada, and K. Uehara, “Photosensitized inactivation of ribonucleic acids in the presence of riboflavin,” BBA Section Nucleic Acids And Protein Synthesis, vol. 103, no. 2, pp. 360–363, 1965. View at: Google Scholar
  6. T. Maisch, J. Baier, B. Franz et al., “The role of singlet oxygen and oxygen concentration in photodynamic inactivation of bacteria,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 17, pp. 7223–7228, 2007. View at: Publisher Site | Google Scholar
  7. P. H. Ruane, R. Edrich, D. Gampp, S. D. Keil, R. L. Leonard, and R. P. Goodrich, “Photochemical inactivation of selected viruses and bacteria in platelet concentrates using riboflavin and light,” Transfusion, vol. 44, no. 6, pp. 877–885, 2004. View at: Publisher Site | Google Scholar
  8. K. Makdoumi, J. Mortensen, and S. Crafoord, “Infectious keratitis treated with corneal crosslinking,” Cornea, vol. 29, no. 12, pp. 1353–1358, 2010. View at: Publisher Site | Google Scholar
  9. S. A. R. Martins, J. C. Combs, G. Noguera et al., “Antimicrobial efficacy of riboflavin/UVA combination (365 nm) in vitro for bacterial and fungal isolates: a potential new treatment for infectious keratitis,” Investigative Ophthalmology and Visual Science, vol. 49, no. 8, pp. 3402–3408, 2008. View at: Publisher Site | Google Scholar
  10. H. P. Iseli, M. A. Thiel, F. Hafezi, J. Kampmeier, and T. Seiler, “Ultraviolet a/riboflavin corneal cross-linking for infectious keratitis associated with corneal melts,” Cornea, vol. 27, no. 5, pp. 590–594, 2008. View at: Publisher Site | Google Scholar
  11. M. Iakovleva and V. Kozel'tsev, “Proteolysis of collagen by several species of micromycetes and spore-forming bacteria,” Prikladnaia Biokhimiia i Mikrobiologiia, vol. 30, pp. 121–126, 1993. View at: Google Scholar
  12. D. Chai, T. Juhasz, D. J. Brown, and J. V. Jester, “Nonlinear optical collagen cross-linking and mechanical stiffening: a possible photodynamic therapeutic approach to treating corneal ectasia,” Journal of Biomedical Optics, vol. 18, no. 3, Article ID 038003, 2013. View at: Publisher Site | Google Scholar
  13. D. P. S. O'Brart, “Corneal collagen cross-linking: a review,” Journal of Optometry, vol. 7, no. 3, pp. 113–124, 2014. View at: Publisher Site | Google Scholar
  14. K. V. Zamora and J. J. Males, “Polymicrobial keratitis after a collagen cross-linking procedure with postoperative use of a contact lens,” Cornea, vol. 28, no. 4, pp. 474–476, 2009. View at: Publisher Site | Google Scholar
  15. C. Koppen, J. C. Vryghem, L. Gobin, and M.-J. Tassignon, “Keratitis and corneal scarring after UVA/riboflavin cross-linking for keratoconus,” Journal of Refractive Surgery, vol. 25, no. 9, pp. S819–S823, 2009. View at: Publisher Site | Google Scholar
  16. J. J. Pérez-Santonja, A. Artola, J. Javaloy, J. L. Alió, and J. L. Abad, “Microbial keratitis after corneal collagen crosslinking,” Journal of Cataract and Refractive Surgery, vol. 35, no. 6, pp. 1138–1140, 2009. View at: Publisher Site | Google Scholar
  17. F. Raiskup and E. Spoerl, “Corneal crosslinking with riboflavin and ultraviolet A. I. principles,” The Ocular Surface, vol. 11, no. 2, pp. 65–74, 2013. View at: Publisher Site | Google Scholar
  18. M. Pollhammer and C. Cursiefen, “Bacterial keratitis early after corneal crosslinking with riboflavin and ultraviolet-A,” Journal of Cataract and Refractive Surgery, vol. 35, no. 3, pp. 588–589, 2009. View at: Publisher Site | Google Scholar
  19. T. Koller, M. Mrochen, and T. Seiler, “Complication and failure rates after corneal crosslinking,” Journal of Cataract and Refractive Surgery, vol. 35, no. 8, pp. 1358–1362, 2009. View at: Publisher Site | Google Scholar
  20. G. D. Kymionis, D. M. Portaliou, D. I. Bouzoukis et al., “Herpetic keratitis with iritis after corneal crosslinking with riboflavin and ultraviolet A for keratoconus,” Journal of Cataract & Refractive Surgery, vol. 33, no. 11, pp. 1982–1984, 2007. View at: Publisher Site | Google Scholar
  21. M. Doors, N. G. Tahzib, F. A. Eggink, T. T. J. M. Berendschot, C. A. B. Webers, and R. M. M. A. Nuijts, “Use of anterior segment optical coherence tomography to study corneal changes after collagen cross-linking,” American Journal of Ophthalmology, vol. 148, no. 6, pp. 844–851.e2, 2009. View at: Publisher Site | Google Scholar
  22. F. Hafezi, J. Kanellopoulos, R. Wiltfang, and T. Seiler, “Corneal collagen crosslinking with riboflavin and ultraviolet A to treat induced keratectasia after laser in situ keratomileusis,” Journal of Cataract and Refractive Surgery, vol. 33, no. 12, pp. 2035–2040, 2007. View at: Publisher Site | Google Scholar
  23. C. Mazzotta, A. Balestrazzi, S. Baiocchi, C. Traversi, and A. Caporossi, “Stromal haze after combined riboflavin-UVA corneal collagen cross-linking in keratoconus: in vivo confocal microscopic evaluation,” Clinical & Experimental Ophthalmology, vol. 35, no. 6, pp. 580–582, 2007. View at: Publisher Site | Google Scholar
  24. F. Raiskup, A. Hoyer, and E. Spoerl, “Permanent corneal haze after riboflavin-UVA-induced cross-linking in keratoconus,” Journal of Refractive Surgery, vol. 25, no. 9, pp. S824–S828, 2009. View at: Publisher Site | Google Scholar
  25. N. S. Gokhale, “Corneal endothelial damage after collagen cross-linking treatment,” Cornea, vol. 30, no. 12, pp. 1495–1498, 2011. View at: Publisher Site | Google Scholar
  26. M. A. Henriquez, L. Izquierdo, C. Bernilla, P. A. Zakrzewski, and M. Mannis, “Riboflavin/ultraviolet a corneal collagen cross-linking for the treatment of keratoconus: visual outcomes and scheimpflug analysis,” Cornea, vol. 30, no. 3, pp. 281–286, 2011. View at: Publisher Site | Google Scholar
  27. C. Wittig-Silva, E. Chan, F. M. A. Islam, T. Wu, M. Whiting, and G. R. Snibson, “A randomized, controlled trial of corneal collagen cross-linking in progressive keratoconus: three-year results,” Ophthalmology, vol. 121, no. 4, pp. 812–821, 2014. View at: Publisher Site | Google Scholar
  28. N. Kato, I. Toda, Y. Hori-Komai, C. Sakai, and K. Tsubota, “Five-year outcome of LASIK for myopia,” Ophthalmology, vol. 115, no. 5, pp. 839–844.e2, 2008. View at: Publisher Site | Google Scholar
  29. M. Lombardo, G. Pucci, R. Barberi, and G. Lombardo, “Interaction of ultraviolet light with the cornea: clinical implications for corneal crosslinking,” Journal of Cataract & Refractive Surgery, vol. 41, no. 2, pp. 446–449, 2015. View at: Publisher Site | Google Scholar
  30. E. Chan and G. R. Snibson, “Current status of corneal collagen cross-linking for keratoconus: a review,” Clinical and Experimental Optometry, vol. 96, no. 2, pp. 155–164, 2013. View at: Publisher Site | Google Scholar
  31. S. Dhawan, K. Rao, and S. Natrajan, “Complications of corneal collagen cross-linking,” Journal of Ophthalmology, vol. 2011, Article ID 869015, 5 pages, 2011. View at: Publisher Site | Google Scholar
  32. S. Garcia-Delpech, M. Díaz-Llopis, P. Udaondo, and D. Salom, “Fusarium keratitis 3 weeks after healed corneal cross-linking,” Journal of Refractive Surgery, vol. 26, no. 12, pp. 994–995, 2010. View at: Publisher Site | Google Scholar
  33. M. Rana, A. Lau, A. Aralikatti, and S. Shah, “Severe microbial keratitis and associated perforation after corneal crosslinking for keratoconus,” Contact Lens and Anterior Eye, vol. 38, no. 2, pp. 134–137, 2015. View at: Publisher Site | Google Scholar
  34. M. A. Al-Amry, “Severe bilateral paralimbal sterile infiltrates after photorefractive keratectomy,” Middle East African Journal of Ophthalmology, vol. 21, no. 1, pp. 83–85, 2014. View at: Publisher Site | Google Scholar
  35. K. J. Wroblewski, J. F. Pasternak, K. S. Bower et al., “Infectious keratitis after photorefractive keratectomy in the United States army and navy,” Ophthalmology, vol. 113, no. 4, pp. 520–525, 2006. View at: Publisher Site | Google Scholar
  36. L. Mastropasqua, “Collagen cross-linking: when and how? A review of the state of the art of the technique and new perspectives,” Eye and Vision, vol. 2, no. 1, 2015. View at: Publisher Site | Google Scholar
  37. L. Mastropasqua, M. Nubile, R. Calienno et al., “Corneal cross-linking: Intrastromal riboflavin concentration in iontophoresis-assisted imbibition versus traditional and transepithelial techniques,” American Journal of Ophthalmology, vol. 157, no. 3, pp. 623–630, 2014. View at: Publisher Site | Google Scholar
  38. G. Wollensak, C. Mazzotta, T. Kalinski, and S. Sel, “Limbal and conjunctival epithelium after corneal cross-linking using riboflavin and UVA,” Cornea, vol. 30, no. 12, pp. 1448–1454, 2011. View at: Publisher Site | Google Scholar
  39. H. Merwald, G. Klosner, C. Kokesch, M. Der-Petrossian, H. Hönigsmann, and F. Trautinger, “UVA-induced oxidative damage and cytotoxicity depend on the mode of exposure,” Journal of Photochemistry and Photobiology B: Biology, vol. 79, no. 3, pp. 197–207, 2005. View at: Publisher Site | Google Scholar
  40. P. J. Rochette, J.-P. Therrien, R. Drouin et al., “UVA-induced cyclobutane pyrimidine dimers form predominantly at thymine-thymine dipyrimidines and correlate with the mutation spectrum in rodent cells,” Nucleic Acids Research, vol. 31, no. 11, pp. 2786–2794, 2003. View at: Publisher Site | Google Scholar
  41. D. E. Brash, J. A. Rudolph, J. A. Simon et al., “A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma,” Proceedings of the National Academy of Sciences of the United States of America, vol. 88, no. 22, pp. 10124–10128, 1991. View at: Publisher Site | Google Scholar
  42. G. P. Pfeifer and A. Besaratinia, “UV wavelength-dependent DNA damage and human non-melanoma and melanoma skin cancer,” Photochemical and Photobiological Sciences, vol. 11, no. 1, pp. 90–97, 2012. View at: Publisher Site | Google Scholar
  43. J. Dahle and E. Kvam, “Induction of delayed mutations and chromosomal instability in fibroblasts after UVA-, UVB-, and X-radiation,” Cancer Research, vol. 63, no. 7, pp. 1464–1469, 2003. View at: Google Scholar
  44. J. Dahle, P. Noordhuis, T. Stokke, D. H. Svendsrud, and E. Kvam, “Multiplex polymerase chain reaction analysis of UV-A- and UV-B-induced delayed and early mutations in V79 Chinese hamster cells,” Photochemistry and Photobiology, vol. 81, no. 1, pp. 114–119, 2005. View at: Publisher Site | Google Scholar
  45. R. P. Phillipson, S. E. Tobi, J. A. Morris, and T. J. McMillan, “UV-A induces persistent genomic instability in human keratinocytes through an oxidative stress mechanism,” Free Radical Biology and Medicine, vol. 32, no. 5, pp. 474–480, 2002. View at: Publisher Site | Google Scholar
  46. E. Sage, P.-M. Girard, and S. Francesconi, “Unravelling UVA-induced mutagenesis,” Photochemical & Photobiological Sciences, vol. 11, no. 1, pp. 74–80, 2012. View at: Publisher Site | Google Scholar
  47. J. C. Yam and A. K. Kwok, “Ultraviolet light and ocular diseases,” International Ophthalmology, vol. 34, no. 2, pp. 383–400, 2014. View at: Publisher Site | Google Scholar
  48. S. Basti and M. S. Macsai, “Ocular surface squamous neoplasia: a review,” Cornea, vol. 22, no. 7, pp. 687–704, 2003. View at: Publisher Site | Google Scholar
  49. A. J. Shortt, G. A. Secker, P. M. Munro, P. T. Khaw, S. J. Tuft, and J. T. Daniels, “Characterization of the limbal epithelial stem cell niche: novel imaging techniques permit in vivo observation and targeted biopsy of limbal epithelial stem cells,” Stem Cells, vol. 25, no. 6, pp. 1402–1409, 2007. View at: Publisher Site | Google Scholar
  50. H. S. Dua and A. Azuara-Blanco, “Autologous limbal transplantation in patients with unilateral corneal stem cell deficiency,” British Journal of Ophthalmology, vol. 84, no. 3, pp. 273–278, 2000. View at: Publisher Site | Google Scholar
  51. W. Li, Y. Hayashida, Y.-T. Chen, and S. C. G. Tseng, “Niche regulation of corneal epithelial stem cells at the limbus,” Cell Research, vol. 17, no. 1, pp. 26–36, 2007. View at: Publisher Site | Google Scholar
  52. H. S. Dua, V. A. Shanmuganathan, A. O. Powell-Richards, P. J. Tighe, and A. Joseph, “Limbal epithelial crypts: a novel anatomical structure and a putative limbal stem cell niche,” British Journal of Ophthalmology, vol. 89, no. 5, pp. 529–532, 2005. View at: Publisher Site | Google Scholar
  53. G. Pellegrini, O. Golisano, P. Paterna et al., “Location and clonal analysis of stem cells and their differentiated progeny in the human ocular surface,” The Journal of Cell Biology, vol. 145, no. 4, pp. 769–782, 1999. View at: Publisher Site | Google Scholar
  54. N. Pinnamaneni and J. L. Funderburgh, “Concise review: stem cells in the corneal stroma,” Stem Cells, vol. 30, no. 6, pp. 1059–1063, 2012. View at: Publisher Site | Google Scholar
  55. F. Majo, A. Rochat, M. Nicolas, G. A. Jaoudé, and Y. Barrandon, “Oligopotent stem cells are distributed throughout the mammalian ocular surface,” Nature, vol. 456, no. 7219, pp. 250–254, 2008. View at: Publisher Site | Google Scholar
  56. K. Higa, S. Shimmura, H. Miyashita, J. Shimazaki, and K. Tsubota, “Melanocytes in the corneal limbus interact with K19-positive basal epithelial cells,” Experimental Eye Research, vol. 81, no. 2, pp. 218–223, 2005. View at: Publisher Site | Google Scholar
  57. G. Wollensak, E. Spoerl, F. Reber, and T. Seiler, “Keratocyte cytotoxicity of riboflavin/UVA-treatment in vitro,” Eye, vol. 18, no. 7, pp. 718–722, 2004. View at: Publisher Site | Google Scholar
  58. G. Wollensak, E. Spoerl, M. Wilsch, and T. Seiler, “Keratocyte apoptosis after corneal collagen cross-linking using riboflavin/UVA treatment,” Cornea, vol. 23, no. 1, pp. 43–49, 2004. View at: Publisher Site | Google Scholar
  59. G. Wollensak, E. Spörl, F. Reber, L. Pillunat, and R. Funk, “Corneal endothelial cytotoxicity of riboflavin/UVA treatment in vitro,” Ophthalmic Research, vol. 35, no. 6, pp. 324–328, 2003. View at: Publisher Site | Google Scholar
  60. T. Koller, S. Schumacher, F. Fankhauser, and T. Seiler, “Riboflavin/ultraviolet a crosslinking of the paracentral cornea,” Cornea, vol. 32, no. 2, pp. 165–168, 2013. View at: Publisher Site | Google Scholar
  61. A. Ringvold, “Corneal epithelium and UV-protection of the eye,” Acta Ophthalmologica Scandinavica, vol. 76, no. 2, pp. 149–153, 1998. View at: Publisher Site | Google Scholar
  62. A. Thorsrud, B. Nicolaissen, and L. Drolsum, “Corneal collagen crosslinking in vitro: inhibited regeneration of human limbal epithelial cells after riboflavin-ultraviolet-a exposure,” Journal of Cataract and Refractive Surgery, vol. 38, no. 6, pp. 1072–1076, 2012. View at: Publisher Site | Google Scholar
  63. H. Matalia, R. Shetty, K. Dhamodaran, M. Subramani, V. Arokiaraj, and D. Das, “Potential apoptotic effect of ultraviolet-A irradiation during cross-linking: a study on ex vivo cultivated limbal epithelial cells,” British Journal of Ophthalmology, vol. 96, no. 10, pp. 1339–1345, 2012. View at: Publisher Site | Google Scholar
  64. J. Vimalin, N. Gupta, M. Jambulingam, P. Padmanabhan, and H. N. Madhavan, “The effect of riboflavin-UV-A treatment on corneal limbal epithelial cells—a study on human cadaver eyes,” Cornea, vol. 31, no. 9, pp. 1052–1059, 2012. View at: Publisher Site | Google Scholar
  65. J. E. Moore, S. D. Atkinson, D. T. Azar et al., “Protection of corneal epithelial stem cells prevents ultraviolet A damage during corneal collagen cross-linking treatment for keratoconus,” British Journal of Ophthalmology, vol. 98, no. 2, pp. 270–274, 2014. View at: Publisher Site | Google Scholar
  66. J. H. Krumeich, B. Brand-Saberi, V. Chankiewitz, E. Chankiewitz, and R. Guthoff, “Induction of neoplasia after deep anterior lamellar keratoplasty in a CXL-treated cornea,” Cornea, vol. 33, no. 3, pp. 313–316, 2014. View at: Publisher Site | Google Scholar
  67. N. S. Agar, G. M. Halliday, R. S. C. Barnetson, H. N. Ananthaswamy, M. Wheeler, and A. M. Jones, “The basal layer in human squamous tumors harbors more UVA than UVB fingerprint mutations: a role for UVA in human skin carcinogenesis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 14, pp. 4954–4959, 2004. View at: Publisher Site | Google Scholar
  68. V. Jeyalatha, M. Jambulingam, N. Gupta, P. Padmanabhan, and H. N. Madhavan, “Study on polymethylmethacrylate ring in protecting limbal stem cells during collagen cross-linking,” Ophthalmic Research, vol. 50, no. 2, pp. 113–116, 2013. View at: Publisher Site | Google Scholar
  69. K. Bilgihan and E. Yuksel, “A new simple corneal limbal protection technique during corneal collagen cross-linking,” Eye & Contact Lens, vol. 41, no. 2, pp. 130–131, 2015. View at: Publisher Site | Google Scholar
  70. R. Shetty, H. Matalia, R. Nuijts et al., “Safety profile of accelerated corneal cross-linking versus conventional cross-linking: a comparative study on ex vivo-cultured limbal epithelial cells,” British Journal of Ophthalmology, vol. 99, pp. 272–280, 2014. View at: Publisher Site | Google Scholar
  71. Y. Çinar, A. K. Cingü, F. M. Türkcü et al., “Comparison of accelerated and conventional corneal collagen cross-linking for progressive keratoconus,” Cutaneous and Ocular Toxicology, vol. 33, no. 3, pp. 218–222, 2014. View at: Publisher Site | Google Scholar
  72. Y. Çınar, A. K. Cingü, F. M. Turkcu et al., “Accelerated corneal collagen cross-linking for progressive keratoconus,” Cutaneous and Ocular Toxicology, vol. 33, no. 2, pp. 168–171, 2014. View at: Publisher Site | Google Scholar
  73. N. Bouheraoua, L. Jouve, V. Borderie, and L. Laroche, “Three different protocols of corneal collagen crosslinking in keratoconus: conventional, accelerated and iontophoresis,” Journal of Visualized Experiments, vol. 2015, no. 105, Article ID e53119, 2015. View at: Publisher Site | Google Scholar
  74. J. Wernli, S. Schumacher, E. Spoerl, and M. Mrochen, “The efficacy of corneal cross-linking shows a sudden decrease with very high intensity UV light and short treatment time,” Investigative Ophthalmology and Visual Science, vol. 54, no. 2, pp. 1176–1180, 2013. View at: Publisher Site | Google Scholar
  75. M. Tomita, M. Mita, and T. Huseynova, “Accelerated versus conventional corneal collagen crosslinking,” Journal of Cataract and Refractive Surgery, vol. 40, no. 6, pp. 1013–1020, 2014. View at: Publisher Site | Google Scholar
  76. J. B. Randleman, S. S. Khandelwal, and F. Hafezi, “Corneal cross-linking,” Survey of Ophthalmology, vol. 60, no. 6, pp. 509–523, 2015. View at: Publisher Site | Google Scholar
  77. A. L. K. Ng, T. C. Chan, and A. C. Cheng, “Conventional versus accelerated corneal collagen cross-linking in the treatment of keratoconus,” Clinical and Experimental Ophthalmology, vol. 44, no. 1, pp. 8–14, 2016. View at: Publisher Site | Google Scholar
  78. C. Caruso, C. Ostacolo, R. L. Epstein, G. Barbaro, S. Troisi, and D. Capobianco, “Transepithelial corneal cross-linking with Vitamin E-enhanced riboflavin solution and abbreviated, low-dose UV-A: 24-month clinical outcomes,” Cornea, vol. 35, no. 2, pp. 145–150, 2016. View at: Publisher Site | Google Scholar
  79. S. Troisi, A. Del Prete, and C. Caruso, “Ophthalmic solution for protecting internal structures of the eyeball against UV-A rays or for the treatment of keratoconus with a trans-epithelial cross-linking technique,” Google Patents, 2015. View at: Google Scholar
  80. J. Dahle, E. Kvam, and T. Stokke, “Bystander effects in UV-induced genomic instability: antioxidants inhibit delayed mutagenesis induced by ultraviolet A and B radiation,” Journal of Carcinogenesis, vol. 4, article 11, 2005. View at: Publisher Site | Google Scholar
  81. C. Meewes, P. Brenneisen, J. Wenk et al., “Adaptive antioxidant response protects dermal fibroblasts from UVA-induced phototoxicity,” Free Radical Biology and Medicine, vol. 30, no. 3, pp. 238–247, 2001. View at: Publisher Site | Google Scholar
  82. J. Tao, M. Abudoukelimu, Y. Ma et al., “Secreted frizzled related protein 1 protects H9C2 cells from hypoxia/re-oxygenation injury by blocking the Wnt signaling pathway,” Lipids in Health and Disease, vol. 15, no. 1, 2016. View at: Publisher Site | Google Scholar
  83. A. Leccisotti and T. Islam, “Transepithelial corneal collagen cross-linking in keratoconus,” Journal of Refractive Surgery, vol. 26, no. 12, pp. 942–948, 2010. View at: Publisher Site | Google Scholar
  84. P. Vinciguerra, R. Mencucci, V. Romano et al., “Imaging mass spectrometry by matrix-assisted laser desorption/ionization and stress-strain measurements in iontophoresis transepithelial corneal collagen cross-linking,” BioMed Research International, vol. 2014, Article ID 404587, 12 pages, 2014. View at: Publisher Site | Google Scholar
  85. V. Soler, M. Cassagne, C. Laurent et al., “Iontophoresis transcorneal delivery technique for transepithelial corneal collagen crosslinking with riboflavin in a rabbit model,” Investigative Ophthalmology & Visual Science, vol. 54, pp. 4299–4299, 2013. View at: Google Scholar
  86. M. Lombardo, S. Serrao, M. Rosati, P. Ducoli, and G. Lombardo, “Biomechanical changes in the human cornea after transepithelial corneal crosslinking using iontophoresis,” Journal of Cataract and Refractive Surgery, vol. 40, no. 10, pp. 1706–1715, 2014. View at: Publisher Site | Google Scholar
  87. D. M. Gore, D. O’Brart, P. French, C. Dunsby, and B. D. Allan, “Transepithelial riboflavin absorption in an ex vivo rabbit corneal model,” Investigative Ophthalmology and Visual Science, vol. 56, no. 8, pp. 5006–5011, 2015. View at: Publisher Site | Google Scholar
  88. G. Bikbova and M. Bikbov, “Transepithelial corneal collagen cross-linking by iontophoresis of riboflavin,” Acta Ophthalmologica, vol. 92, no. 1, pp. e30–e34, 2014. View at: Publisher Site | Google Scholar
  89. P. Vinciguerra, J. B. Randleman, V. Romano et al., “Transepithelial iontophoresis corneal collagen cross-linking for progressive keratoconus: initial clinical outcomes,” Journal of Refractive Surgery, vol. 30, no. 11, pp. 746–753, 2014. View at: Publisher Site | Google Scholar
  90. S. Rossi, A. Orrico, C. Santamaria et al., “Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking,” Clinical Ophthalmology, vol. 9, pp. 503–509, 2015. View at: Publisher Site | Google Scholar
  91. N. Soeters, R. P. L. Wisse, D. A. Godefrooij, S. M. Imhof, and N. G. Tahzib, “Transepithelial versus epithelium-off corneal cross-linking for the treatment of progressive keratoconus: a randomized controlled trial,” American Journal of Ophthalmology, vol. 159, no. 5, article 9237, pp. e821–e828, 2015. View at: Publisher Site | Google Scholar
  92. M. Filippello, E. Stagni, and D. O'Brart, “Transepithelial corneal collagen crosslinking: bilateral study,” Journal of Cataract & Refractive Surgery, vol. 38, no. 2, pp. 283–291, 2012. View at: Publisher Site | Google Scholar
  93. A. Magli, R. Forte, A. Tortori, L. Capasso, G. Marsico, and E. Piozzi, “Epithelium-off corneal collagen cross-linking versus transepithelial cross-linking for pediatric keratoconus,” Cornea, vol. 32, no. 5, pp. 597–601, 2013. View at: Publisher Site | Google Scholar
  94. H. A. Khairy, H. M. Marey, and A. F. Ellakwa, “Epithelium-on corneal cross-linking treatment of progressive keratoconus: a prospective, consecutive study,” Clinical Ophthalmology, vol. 8, pp. 819–823, 2014. View at: Publisher Site | Google Scholar
  95. M. Kim, A. Takaoka, Q. V. Hoang, S. L. Trokel, and D. C. Paik, “Pharmacologic alternatives to riboflavin photochemical corneal cross-linking: a comparison study of cell toxicity thresholds,” Investigative Ophthalmology and Visual Science, vol. 55, no. 5, pp. 3247–3257, 2014. View at: Publisher Site | Google Scholar
  96. A. L. Marcovich, A. Brandis, O. Daphna et al., “Stiffening of rabbit corneas by the bacteriochlorophyll derivative WST11 using near infrared light,” Investigative Ophthalmology and Visual Science, vol. 53, no. 10, pp. 6378–6388, 2012. View at: Publisher Site | Google Scholar
  97. J. Voke, “Radiation effects on the eye, part 3b—ocular effects of ultraviolet radiation,” Optometry Today, vol. 1, pp. 37–40, 1999. View at: Google Scholar
  98. D. Cherfan, E. E. Verter, S. Melki et al., “Collagen cross-linking using rose bengal and green light to increase corneal stiffness,” Investigative Ophthalmology and Visual Science, vol. 54, no. 5, pp. 3426–3433, 2013. View at: Publisher Site | Google Scholar
  99. D. C. Paik, M. R. Solomon, Q. Wen, N. J. Turro, and S. L. Trokel, “Aliphatic β-nitroalcohols for therapeutic corneoscleral cross-linking: chemical mechanisms and higher order nitroalcohols,” Investigative Ophthalmology & Visual Science, vol. 51, no. 2, pp. 836–843, 2010. View at: Publisher Site | Google Scholar
  100. X. Li, Y. Li, Y. Rao, M. R. Solomon, D. C. Paik, and N. J. Turro, “Mechanistic and catalytic studies of β-nitroalcohol crosslinking with polyamine,” Journal of Applied Polymer Science, vol. 128, no. 6, pp. 3696–3701, 2013. View at: Publisher Site | Google Scholar
  101. M. Wang, “Effect of glyceraldehyde cross-linking on a rabbit bullous keratopathy model,” Journal of Ophthalmology, vol. 2015, Article ID 171690, 5 pages, 2015. View at: Publisher Site | Google Scholar
  102. M. Y. Avila, V. A. Gerena, and J. L. Navia, “Corneal crosslinking with genipin, comparison with UV-riboflavin in ex-vivo model,” Molecular Vision, vol. 18, pp. 1068–1073, 2012. View at: Google Scholar
  103. T.-X. Liu and Z. Wang, “Collagen crosslinking of porcine sclera using genipin,” Acta Ophthalmologica, vol. 91, no. 4, pp. e253–e257, 2013. View at: Publisher Site | Google Scholar

Copyright © 2016 Johnny E. Moore et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.