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Volume 2012 (2012), Article ID 653465, 7 pages
Itraconazole Niosomes Drug Delivery System and Its Antimycotic Activity against Candida albicans
1Department of Pharmaceutics, R. C. Patel Institute of Pharmaceutical Education and Research, Maharashtra, Shirpur 425405, India
2Formulation and Development Department, Shreya Life Sciences Pvt. Ltd., MIDC, Waluj, Maharashtra, Aurangabad 431001, India
Received 23 October 2012; Accepted 11 November 2012
Academic Editors: K. Goracinova and M. R. Jaafari
Copyright © 2012 Vijay D. Wagh and Onkar J. Deshmukh. 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.
Niosomes have potential applications in topical drug delivery system. The objective of the study was to formulate and evaluate the niosome of Itraconazole. Surfactant : cholesterol ratio and quantity of ethanol used were studied by applying factorial design. Formulated niosomes were evaluated for vesicle size, entrapment efficiency, drug release, skin permeation, and antimycotic activity. Vesicle size, entrapment efficiency, and drug release were markedly dependent on surfactant : cholesterol ratio and quantity of ethanol used. Permeation of the drug through the skin was affected by cholesterol content in formulation. Itraconazole niosome were having larger zone of inhibition than marketed formulation when activity was checked against C. albicans. Niosomes may be a promising carrier for topical delivery of Itraconazole especially due to their simple production.
Most antifungal drug substances are lipophilic compounds, which are practically insoluble in water . For skin care and the topical treatment of dermatological disease, a wide choice of vehicles ranging from solids to semisolids and liquid preparations is available to clinicians and patients . Topical application of antimicrobial agents is a useful tool for the therapy of skin and soft-tissue infections . A number of strategies to deliver antifungal using nanocarriers are developed to facilitate drug targeting infected cells. Nanosized carriers have been receiving special attention with the aim of minimizing the side effects and improving efficacy of drug therapy. Several nanosized delivery systems have already proved their effectiveness in antifungal therapy . The total therapeutic effect of percutaneous preparations depends not only on the action of the drug itself, but also on other factors related to the structure of the vehicle. Taking into account the peculiarities of fungal parasites, the focus is placed particularly on lipid-based vehicles, and earlier studies have shown that results in improved antifungal activity . Many techniques have been aimed to disrupt and weaken the highly organized intercellular lipids in an attempt to enhance drug transport across the intact skin; one of them is the vesicle formulation as skin delivery system [5–8].
Niosomes have been recognized as a good vehicles for the topical delivery of drugs . They serve as “organic” solvent for the solubilization of poorly soluble drugs, for instances corticosteroids; as a result, higher local drug concentrations at the maximum thermodynamic activity can be applied. They may serve as a local depot for the sustained release of dermal active compounds including antibiotics, corticosteroids, or retinoic acid. By virtue of penetration of individual phospholipid molecules or nonionic ether surfactants into the lipid layers of the stratum corneum and epidermis, they may serve as penetration enhancer and facilitate dermal delivery leading to higher localized drug concentrations. They may serve as rate-limiting membrane barrier for the modulation of systemic absorption, that is, they may serve as controlled transdermal delivery systems.
Mainly two types of vesicle skin interactions occurs during in vitro studies using human skin which may induce various effects on dermal or transdermal drug delivery [10–12]. First, the vesicles in contact with stratum corneum aggregate fuse and adhere to the cell surface. It is believed that this interaction leads to a high thermodynamic activity gradient of the drug at the vesicle stratum corneum interface, which is the driving force for penetration of the lipophilic drugs across the stratum corneum. Secondly, this type of interaction involves the ultrastructural changes of the intercellular lipid regions of the stratum corneum and its deeper layers at maximum depth of about 10 μm as revealed by freeze fracture electron microscopy (FFEM) and Small Angle X-ray Scattering (SAXS).
Itraconazole is synthetic triazole and 1 : 1 : 1 : 1 racemic mixture of four diastereoisomers (two enantiomeric pairs), each possessing 3 chiral centres. The structural formula is closely related to the imidazole and ketoconazole. Itraconazole is a drug of choice for patients with indolent, nonmeningeal infections due to B. dermatitidis, H. capsulatum, P. brasiliensis, and C. immitis. Approximately half of the patients with distal subungual onychomycosis respond well to Itraconazole. Itraconazole is often the best choice for the treatment of pseudallescheriasis, an infection not responding to the amphotericin B therapy, as well as cutaneous or extracutaneous sporotrichosis, tinea corporis, and extensive tinea versicolor. Itraconazole is used in the treatment of toenail onychomycosis with terbinafine as one week per month for three months. Itraconazole has low solubility and low permeation. By incorporation of Itraconazole in small niosomes, the drug can be targeted directly to the site of action, thus enhancing its therapeutic efficacy.
2. Materials and Methods
Itraconazole was received as a gift sample from USV Ltd., Mumbai, India. Span 60 was purchased from Loba Chemie Private Ltd. Cholesterol AR (Mol. Wt.—386.6 D) was purchased from Qualigens fine chemicals Ltd., India. Ethanol Propanol were obtained from Research Lab Chem, Mumbai. Other chemicals were pharmacopeial grade or A.R. grade. Fresh distilled water was used for all the formulation.
2.2. Formulation of Niosomes
Niosomes were prepared by hydration of proniosome . Precisely, surfactants : cholesterol (total surfactant 500 mg) and drug (50 mg) were taken in a clean and dry, wide mouth small glass vial. The surfactants : cholesterol ratio and quantity of ethanol used in formulation were as per the factorial design. Compositions of 9 batches of niosomes are given in Table 1. After mixing all the ingredients, the open end of the glass tube was covered with a lid to prevent loss of solvent from it and warmed on a water bath at 60–70°C for about 5 min, until the surfactants were dissolved completely. The aqueous phase (0.1% glycerol solution) was added and warmed on a water bath till clear solution is formed on cooling converts into niosomal formulation. The dispersion obtained was preserved in same glass tube in dark for characterization.
2.3. Size, Shape, and Morphological Characterization 
Vesicular structure of surfactant-based vesicles can be visualized by microscope. Size of the niosomes prepared from proniosomes can be analyzed by 3 different method, namely, agitations (shaking) without agitation and with sonication. Optical microscope with digital camera (catcham) was used to study size, shape, and morphology of niosomes.
2.4. Entrapment Efficiency 
The Analysis of entrapment efficiency can be done by centrifugation method. The niosome entrapped drug was separated from the free drug by the centrifugation method. The prepared niosomal dispersion was subjected for centrifugation at high 7000 rpm for 30 min. Clear supernatant liquid was separated from niosomes. Niosomes were disrupted and analyzed by using spectrophotometer to calculate the amount of entrapped drug:
2.5. In Vitro Drug Release
Drug release from niosome was tested with modified Keshary-Chien diffusion cell (receptor compartment capacity 20 mL), using cellophane membrane with permeation area of 2.54 cm2. 20 mL of release medium (15 mL 7.4 phosphate buffer and 5 mL methanol) was added to the acceptor chamber. The prepared niosomal dispersion was subjected for centrifugation at high 7000 rpm for 30 min to separate the unentrapped drug. Niosomes encapsulating drug equivalent to 50 mg was placed in donor compartment. The entire assembly was kept on a magnetic stirrer and was maintained at . At predetermined time points, 1 mL samples were withdrawn from the acceptor compartment, replacing the sampled volume with release medium after each sampling for a period of 6 hrs. The samples were suitably diluted with solvent (chloroform 1 : 4 v/v and filled up with methanol 3 : 4 v/v) and measured spectrophotometrically at 260 nm.
2.6. In Vitro Skin Permeation Study 
The Wistar rat was given free access to food and water 24 hr. The hair was removed by hair clipper. The rat was killed by respiratory paralysis. The abdominal skin was carefully excise and fatty layer, debris, was carefully removed. The skin was washed with saline solution and used within 24 hr. The skin was mounted on Modified Keshary-Chien diffusion cell with permeation area of 2.54 cm2 (receptor compartment capacity 20 mL) with stratum corneum facing donor compartment. 20 mL of release medium (15 mL 7.4 phosphate buffer and 5 mL methanol) was added to the acceptor chamber. The prepared niosomal dispersion was subjected for centrifugation at high 7000 rpm for 30 min to separate the unentrapped drug. Niosomes encapsulating drug equivalent to 50 mg was placed in donor compartment. Niosomes encapsulating drug equivalent to 50 mg was placed in donor compartment. The entire assembly was kept on a magnetic stirrer and was maintained at . At predetermined time points, 1 mL samples were withdrawn from the acceptor compartment, replacing the sampled volume with release medium after each sampling for a period of 8 hrs. The samples were suitably diluted with solvent (chloroform 1 : 4 v/v and filled up with methanol 3 : 4 v/v) and measured spectrophotometrically at 260 nm.
2.7. In Vitro Antimycotic Study 
Agar-cup diffusion method was adopted. These tests were carried out using cultures of Candida albicans (AJ 005123) (0.1%), in Sabouraud dextrose agar. Active culture of Candida albicans strain was inoculated in sterile 0.85% NaCl tube in a ratio of 1 : 9. Further dilution of the culture where prepared in a sterile 0.85% NaCl to get 106 CFU/mL. Seeding of culture performed by swabbing method in which sterile swab was dipped into the culture suspension and excess fluid removed by pressing gently against the wall of test tube. Swab was placed on the edge of the agar plate and move across to the other sides, this was separated to obtain an even spread in sterile conditions. Using borer, wells were made in the seeded agar plates of 6 mm diameter and to it ES60A to ES60I encapsulating 20 mg of itraconazole and 200 mg of marketed formulation (1%) were added. Plates were kept in freezer for diffusion for 10–15 min. And then placed in incubator for incubation period of 24–48 hr at 37°C. Results were seen as diameter of zone of inhibition and compared with that of empty niosomal formulation and marketed formulation (Itral).
3. Results and Discussions
The method of preparation of proniosomes is based on the simple idea that the mixture of surfactant:alcohol:aqueous phase can be used to form the concentrated proniosomal gel, which can be converted to a stable niosomal dispersion by dilution with excess aqueous phase. This technique involves the principle of coacervation-phase separation .
3.1. Vesicle Characteristics
Optical microscope with digital camera (catcham) was used to study size, shape, and morphology of niosomes. Vesicles were found to be spherical, discrete, and multilammelar. Results are represented in Table 2. Size of vesicles was found to be in the order of hydration: without agitation > with agitation > with ultrasonication. Batch ESC60C ( μm) has shown the largest size vesicles were formed after hydration of proniosomes without agitation. Whereas, ES60 G ( μm) with shaking and ES60 G ( μm) after sonication (Ultrasonic cleaner, Trans-o-sonic, Lab Hosp, Mumbai) has shown the smaller vesicles. This might be due to energy applied during agitation, and ultrasonication results in their breakage into smaller vesicles; ultrasonication energy being highest results in small unilamellar vesicles . These results states that increase in cholesterol content increases hydrophobicity. Increased hydrophobicity decreases surface energy which subsequently reduces vesicle size [16–20]. The polydispersity index was always found to be very low, showing that formulated niosome are uniform in size .
3.2. Entrapment Efficiency (%)
Table 3 represents entrapment efficiency % of various formulation batches. With increasing cholesterol, the bilayer hydrophobicity and stability increased [21, 22] and permeability decreased  which lead to efficiently trapping the hydrophobic drug into bilayers as vesicles formed. Entrapment efficiency was decreased with increase in cholesterol ratio above a certain limit may be due to the fact that increasing cholesterol beyond a certain concentration can disrupt the regular linear structure of vesicular membranes . Entrapment efficiency has an impact on solubility of drug in the alcohol. Entrapment efficiency increased with the increase in alcohol quantity.
3.3. In Vitro Drug Release
In vitro Drug release was represented by Figures 1, 2, and 3. The rate of release was in the order ES60D < ES60E < ES60F < ES60H < ES60G < ES60I < ES60A < ES60B < ES60C. Increasing the cholesterol content resulted in more intact lipid bilayers as a barrier for drug release and decreased its leakage by improving the fluidity of the bilayer membrane and reducing its permeability, which led to lower drug elution from the vesicles. When the cholesterol content increased above a certain limit, the release rate increased due to the fact that increasing cholesterol beyond a certain concentration can disrupt the regular linear structure of vesicular membranes [24, 25].
3.4. Multiple Regression Analysis of Factorial Design
The responses of factorial design Y1 (vesicle size) and Y2 (encapsulation efficiency %) were subjected to multiple regression analysis by PCP DISSO software. Surface response plots (as shown in Figures 4, 5, and 6) and coefficient values indicate both independent variables X1 (surfactant : cholesterol) and X2 (quantity of alcohol used) affect responses (Tables 4 and 5).
3.5. Skin Permeation Studies
Figure 7 shows the percent of drug permeated after 6 hr through skin form; it was in the order ES60A > ES60G > ES60D. Increasing the cholesterol content resulted in decreased permeation of Itraconazole. When the cholesterol content increased above certain limit, permeation is increased due to the fact that increasing cholesterol beyond a certain concentration can disrupt the regular linear structure of vesicular membranes [25–27]. Amount of alcohol used in formulation has no significant effect on permeation.
3.6. Antimycotic Study of Formulated Niosomes
Figure 8 represents zone of inhibition of formulated niosome batches and marketed formulation (Itral). Zone of inhibition of niosome formulatio showed that they are more (90 × effective than marketed formulation (Itral)). The empty niosomal formulation was not shown in the zone of inhibition and antimycotic action.
Formulated niosomes were evaluated foe vesicle size, entrapment efficiency, drug release, skin permeation, and antimycotic activity. Vesicle size, entrapment efficiency, and drug release were dependent on surfactant : cholesterol ration and quantity of ethanol used. Formulated niosomes were having a good skin permeation and were more effective in antimycotic activity when compared against marketed formulation. Niosome may be a promising carrier for topical delivery of Itraconazole.
Conflict of Interests
The authors declare that they do not have any financial and personal relationships with other people or organisations that could inappropriately influence (bias) their work.
- P. Puranajoti, R. T. Patil, P. D. Sheth, G. Bommareddy, P. Dondeti, and K. Egbaria, “Design and development of topical microemulsion for poorly water-soluble antifungal agents,” Journal of Applied Research, vol. 2, no. 1, pp. 27–28, 2002.
- H. M. El Laithy and K. M. F. El-Shaboury, “The development of Cutina lipogels and gel microemulsion for topical administration of fluconazole,” AAPS Pharmacetical Science Technology, vol. 3, no. 4, p. 35, 2002.
- S. Mukherjee, S. Ray, and R. S. Thakur, “Design and evaluation of Itraconazole loaded solid lipid nanoparticulate system for improving the antifungal therapy,” Pakistan Journal of Pharmaceutical Sciences, vol. 22, no. 2, pp. 131–138, 2009.
- H. Schreier, “Liposomes and niosomes as topical drug carriers: dermal and transdermal drug delivery,” Journal of Controlled Release, vol. 30, no. 1, pp. 1–15, 1994.
- R. Arora and C. P. Jain, “Advances in niosome as a drug carrier: a review,” Asian Journal of Pharmaceutics, vol. 1, pp. 29–39, 2007.
- Y. Dan-Bo, Z. Jia-Bi, L. Rui-Qin, H. Zhi-Qiang, and S. Jin-Qiu, “Liquid chromatographic method for determination of free and niosome-entrapped nimodipine in mouse plasma and different tissues,” Analytical Letters, vol. 41, no. 4, pp. 533–542, 2008.
- R. A. R. Naresh, G. K. Pillai, N. Udupa, and G. Chandrashekar, “Anti-inflammatory activity of niosome encapsulated diclofenac sodium in arthritic rats,” Indian Journal of Pharmacology, vol. 26, no. 1, pp. 46–48, 1994.
- C. P. Jain, S. P. Vyas, and V. K. Dixit, “Niosomal system for delivery of rifampicin to lymphatics,” Indian Journal of Pharmaceutical Sciences, vol. 68, no. 5, pp. 575–578, 2006.
- A. Manosroi, P. Jantrawut, and J. Manosroi, “Anti-inflammatory activity of gel containing novel elastic niosomes entrapped with diclofenac diethylammonium,” International Journal of Pharmaceutics, vol. 360, no. 1-2, pp. 156–163, 2008.
- J. A. Bouwstra, H. E. H. Hofland, F. Spies, G. S. Gorrisand, and H. E. Junginger, “Liposomes and human stratum corneum in vitro,” in Drug Targeting and Delivery Concepts in Dosage form Design, H. E. Junginger, Ed., vol. 1, p. 205, Ellio Horwood, Chichester, UK, 1992.
- H. E. Junginger, H. E. J. Hofland, and J. A. Bouwstra, “Liposomes and niosomes: interaction with human skin,” Cosmetics & Toiletries, vol. 106, pp. 45–50, 1991.
- E. Touitou, H. E. Junginger, N. D. Weiner, T. Nagai, and M. Mezei, “Liposomes as carriers for topical and transdermal delivery,” Journal of Pharmaceutical Sciences, vol. 83, no. 9, pp. 1189–1203, 1994.
- S. Perrett, M. Golding, and W. P. Williams, “A simple method for the preparation of liposomes for pharmaceutical applications: characterization of the liposomes,” Journal of Pharmacy and Pharmacology, vol. 43, no. 3, pp. 154–161, 1991.
- B. Vora, A. J. Khopade, and N. K. Jain, “Proniosome based transdermal delivery of levonorgestrel for effective contraception,” Journal of Controlled Release, vol. 54, no. 2, pp. 149–165, 1998.
- D. I. Nesseem, “Formulation and evaluation of itraconazole via liquid crystal for topical delivery system,” Journal of Pharmaceutical and Biomedical Analysis, vol. 26, no. 3, pp. 387–399, 2001.
- I. A. Alsarra, A. A. Bosela, S. M. Ahmed, and G. M. Mahrous, “Proniosomes as a drug carrier for transdermal delivery of ketorolac,” European Journal of Pharmaceutics and Biopharmaceutics, vol. 59, no. 3, pp. 485–490, 2005.
- A. T. Yoshioka, B. B. Sternberg, and A. T. Florence, “Preparation and properties of vesicles (niosomes) of sorbitan monoesters (Span 20, 40, 60 and 80) and a sorbitan triester (Span 85),” International Journal of Pharmaceutics, vol. 105, no. 1, pp. 1–6, 1994.
- V. Dubey, D. Mishra, and N. K. Jain, “Melatonin loaded ethanolic liposomes: physicochemical characterization and enhanced transdermal delivery,” European Journal of Pharmaceutics and Biopharmaceutics, vol. 67, no. 2, pp. 398–405, 2007.
- J. A. Barry and K. Gawrisch, “Direct NMR evidence for ethanol binding to the lipid-water interface of phospholipid bilayers,” Biochemistry, vol. 33, no. 26, pp. 8082–8088, 1994.
- V. D. Wagh and O. J. Deshmukh, “Niosomes as a ophthalmic drug delivery system: a review,” Journal of Pharmacy Research, vol. 3, no. 7, pp. 1558–1563, 2010.
- C. Bernsdorff, A. Wolf, R. Winter, and E. Gratton, “Effect of hydrostatic pressure on water penetration and rotational dynamics in phospholipid-cholesterol bilayers,” Biophysical Journal, vol. 72, no. 3, pp. 1264–1277, 1997.
- K. Muppidi, A. S. Pumerantz, J. Wang, and G. Betagiri, “Development and stability studies of novel liposomal vancomycin formulations,” ISRN Pharmaceutics, vol. 2, pp. 1–8, 2012.
- D. Bitounis, R. Fanciullino, A. Iliadis, and J. Ciccolini, “optimizing druggability through liposomal formulation: new approaches to an old concept,” ISRN Pharmaceutics, vol. 2, pp. 1–11, 2012.
- M. S. El-Samaligy, N. N. Afifi, and E. A. Mahmoud, “Increasing bioavailability of silymarin using a buccal liposomal delivery system: preparation and experimental design investigation,” International Journal of Pharmaceutics, vol. 308, no. 1-2, pp. 140–148, 2006.
- M. Mokhtar, O. A. Sammour, M. A. Hammad, and N. A. Megrab, “Effect of some formulation parameters on flurbiprofen encapsulation and release rates of niosomes prepared from proniosomes,” International Journal of Pharmaceutics, vol. 361, no. 1-2, pp. 104–111, 2008.
- J. Y. Fang, S. Y. Yu, P. C. Wu, Y. B. Huang, and Y. H. Tsai, “In vitro skin permeation of estradiol from various proniosome formulations,” International Journal of Pharmaceutics, vol. 215, no. 1-2, pp. 91–99, 2001.
- T. M. Kalyankar, M. Khan, T. Nalanda Rangari, and D. Vijay Wagh, “Novel possibilities of development and therapeutic applications of liposomes,” Journal of Pharmacy Research, vol. 3, no. 8, pp. 1880–1884, 2010.