Disposition Kinetics of Taxanes in Peritoneal Dissemination

Miyamoto, Ken'ichi; Shimada, Tsutomu; Sawamoto, Kazuki; Sai, Yoshimichi; Yonemura, Yutaka

doi:https://doi.org/10.1155/2012/963403

Gastroenterology Research and Practice

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Volume 2012 | Article ID 963403 | https://doi.org/10.1155/2012/963403

Disposition Kinetics of Taxanes in Peritoneal Dissemination

Ken'ichi Miyamoto,¹Tsutomu Shimada,¹Kazuki Sawamoto,¹Yoshimichi Sai,¹and Yutaka Yonemura¹

Academic Editor: Yan Li

Received06 Jan 2012

Accepted14 Feb 2012

Published16 May 2012

Abstract

Treatment of cancers in the abdominal cavity, such as peritoneal dissemination, is difficult, but in principle intraperitoneal administration of anticancer drugs is expected to be preferable to systemic administration. Taxane anticancer drugs are used to treat gastric cancer patients with peritoneal dissemination. They are administered as micellar preparations, Taxol and Taxotere, which consist of paclitaxel in Cremophor EL (crEL) and docetaxel in Polysorbate-80 (PS-80), respectively. In this paper we review the disposition kinetics of taxane anticancer drugs after intraperitoneal administration in peritoneal dissemination patients and animal models and also discuss the effect of the surfactant vehicle on the behavior of taxanes.

1. Introduction

Taxane alkaloids, paclitaxel and docetaxel, are widely used in the treatment of various cancers. Their anticancer activity is related to stabilization of microtubule assembly, and they cause mitotic arrest in the G₂M phase of the cell cycle [1]. Paclitaxel and docetaxel have similar chemical and physical characteristics, as shown in Figure 1, and are barely soluble in various solvents. They are therefore used as micellar preparations, Taxol and Taxotere, which consist of paclitaxel in Cremophor EL (crEL) and docetaxel in Polysorbate-80 (PS-80), respectively (Figure 2).

Chemotherapy for patients with peritoneal dissemination has generally been unsatisfactory. Peritoneal cancer occurs in about 10–15% of patients with gastric cancer and in about 50–60% of relapsed cases after gastrectomy. In general, however, treatment of the peritoneal cancer is ineffective, and the 5-year survival rate is extremely low even after multidisciplinary treatment, such as surgical resection, radiotherapy, and chemotherapy. In most cases, anticancer drugs have been given by systemic administration. But, the peritoneal cavity acts as a sanctuary against systemic chemotherapy because of the existence of a blood-peritoneal barrier consisting of stromal tissue between mesothelial cells and submesothelial blood capillaries [2]. Thus, inadequate therapeutic effects might be due at least in part to failure of the drugs to reach abdominal cancerous tissues at sufficient concentration to eradicate the cancer. The intraperitoneal (i.p.) dosage route might be better than systemic administration for treatment of peritoneal dissemination, and it would be expected to produce a higher drug concentration in the abdominal cavity and to exhibit a lower systemic toxicity compared with intravenous (i.v.) administration. Fushida et al. [3, 4] and Yonemura et al. [5] tried the i.p. infusion of taxane anticancer drugs in gastric cancer patients with peritoneal dissemination and reported that the treatment was more effective, with fewer side effects, than systemic i.v. administration. Sugarbaker et al. [6] have reviewed perioperative intraperitoneal chemotherapy; they noted that the ratio of the area under the drug concentration-time curve (AUC) in the peritoneal cavity and AUC in plasma (AUC_a/AUC_p) was much larger for paclitaxel and docetaxel than for other anticancer drugs, suggesting that taxanes may be effective when used in early postoperative intraperitoneal chemotherapy, without severe systemic toxicity. Moreover, i.p. docetaxel appeared to be more effective than paclitaxel on peritoneal dissemination. Here, we review the disposition kinetics of taxanes after i.p. administration of taxane preparations and discuss the relationship between the pharmacokinetic characteristics and anticancer effects of taxanes, as well as the influence of the micellar surfactant vehicles.

2. Disposition Kinetics in Patients withPeritoneal Cancers

We investigated changes of taxane concentration in the abdominal cavity and peripheral blood after i.p. administration in advanced gastric cancer patients with peritoneal dissemination [7]. Taxol (120 mg, 180 mg) or Taxotere (60 mg, 80 mg) was dissolved in 1 L of physiological saline (final concentration of surfactant; crEL: 1.1–1.6% for Taxol, PS-80: 0.15–0.2% for Taxotere). and the preparation was infused into the peritoneal cavity of nine patients for 1 h. Blood and ascites samples were collected at designated time intervals, and the concentrations of paclitaxel and docetaxel were measured using a modification of the high-performance liquid chromatography method of Vergniol et al. [8] and Loos et al. [9].

When Taxol (120 and 180 mg) was intraperitoneally infused at a volume of 1 L for 1 h, the maximum peritoneal concentrations of paclitaxel just after the infusion were about 110 and 190 μg/mL, respectively, and decreased to 16 and 19 μg/mL, respectively, after 24 h. The plasma concentration reached maximum levels of 38 and 54 ng/mL, respectively, within 3 h after the infusion and fell below the detection limit (5 ng/mL) after 24 h. On the other hand, after 1 h infusion of Taxotere (60 and 80 mg/L), the maximum peritoneal concentrations of docetaxel were 29 and 40 μg/mL, respectively. These concentrations were about a half of the calculated initial concentration of docetaxel, suggesting that the drug was distributed to the peritoneal tissues or elsewhere during infusion. The peritoneal concentration was about 1 to 6 μg/mL after 24 h. The plasma concentration reached the maximum levels of about 112 and 144 ng/mL, respectively, within 2 h after the infusion, then decreased to 5 to 10% of the maximum after 24 h.

Calculation of the pharmacokinetic parameters in ascitic fluid indicated that the distribution volume (Vd_a) and the clearance (CL_a) of docetaxel were two to three times than those of paclitaxel. Among the pharmacokinetic parameters in plasma of these drugs, Vd_p, and CL_p of paclitaxel were larger than those of docetaxel, but the AUC_p, 0−25 of docetaxel tended to be larger than that of paclitaxel. The ratio of AUC in ascitic fluid and AUC in plasma (AUC_a/AUC_p) was 500 to 1700 for paclitaxel and 50 to 100 for docetaxel (Table 1). Similarly, it has been reported that the AUC_a/AUC_p of paclitaxel (about 1,000) [10, 11] was larger than that of docetaxel (about 200) [12, 13] after i.p. infusion. These results suggest that after infusion of taxane preparations into the peritoneal cavity, docetaxel is more easily transferred to peripheral blood vessels than paclitaxel. Namely, after i.p. infusion of Taxol the peritoneal concentration of paclitaxel was well maintained for a long time and permeation into the systemic circulation was low, suggesting that paclitaxel should be effective against peritoneal cancers, and side effects, such as bone marrow depression, should be weak. In the case of intraperitoneally administered Taxotere, the concentrations of docetaxel in the peritoneal cavity and peripheral plasma were above the cytotoxic concentration (in vitro IC₅₀: 4–35 ng/mL) [14], so this anticancer drug may exhibit anticancer action against peritoneal cancers but may also cause systemic side effects.

3. Disposition Kinetics in Peritoneal Dissemination Tumor Model Animals

The rat ascites hepatoma cell line AH130 was established as transplantable tumor by Yoshida [16]. This cell line is maintained by i.p. passage at weekly intervals in female Donryu rats and is widely used to prepare animal models of peritoneal cancer dissemination. The pharmacokinetic behavior of taxane anticancer drugs and the effects of their micellar formulation vehicles have been studied using this model [15]. Four-week-old female Donryu rats were inoculated with 2 × 10⁶ AH130 cells into the peritoneal cavity and used for experiments after 1 to 2 weeks, following an overnight fast. Taxol or Taxotere was given by i.p. injection at a dose of 40 mg/kg in a 20 mL volume containing 0.2% blue dextran as a volume marker; the resulting peritoneal solutions contained 4.2% crEL for paclitacel and 1.5% PS-80 for docetaxel, which are close to the concentrations used in the case of i.v. injection of taxanes in the clinic. In the case of i.v. injection, 5 mg/kg of each drug in a volume of 200 μL was administered by bolus injection into the tail vein. After i.p. or i.v. administration of taxanes to the AH130-bearing rats, the concentrations of drugs in ascitic fluid, free cancer cells, and plasma obtained from the jugular vein were measured at designated time intervals. Solid cancers in the peritoneal cavity were excised after the rats had been killed by decapitation, and the drugs were extracted and their concentrations were measured.

After i.p. administration of taxanes, the ascitic concentration of paclitaxel decayed very slowly, whereas that of docetaxel decreased rapidly. The plasma concentrations of both drugs were very low, but that of paclitaxel increased until 4 h and then remained at a plateau, while that of docetaxel reached the maximum at 1.5 h and then decreased (Figure 3). The values of AUC_p, 0–24 h, and AUC_a, 0–24 h of paclitaxel were significantly larger, by about 2- and 6-fold, respectively, than those of docetaxel, and the apparent first-order absorption rate constant from the peritoneal cavity (ka) of paclitaxel was extremely small (Table 2). The AUC_a/AUC_p ratio of paclitaxel was much larger than that of docetaxel. These results indicate that paclitaxel was retained at much higher concentration than docetaxel in the peritoneal cavity after i.p. administration of taxane preparations, and the transfer of paclitaxel into the systemic circulation was much lower than that of docetaxel, in agreement with clinical findings [7, 10–13]. Figure 4 shows the changes of taxane concentration in free cancer cells in the peritoneal cavity after i.p. administration of Taxol and Taxotere (each 40 mg/kg). The concentration of paclitaxel was very low after Taxol administration, while that of docetaxel was high just after Taxotere administration and then decreased gradually in parallel with the decay of the peritoneal concentration. On the other hand, at 1 h after i.p. administration, the concentration of paclitaxel in solid cancer tissue growing in the peritoneum ( μg/g tissue) was lower than that of docetaxel ( μg/g tissue). Figure 5 shows the apparent concentration ratio in solid cancer tissue versus plasma (Kp, app) 1 h after i.p. or i.v. administration. No marked difference was observed between the Kp,app values of these drugs after i.p. administration, but after i.v. administration the Kp, app of paclitaxel was significantly smaller than that of docetaxel. These results indicate that after i.p. administration of Taxol, paclitaxel was retained at high concentration in the peritoneal cavity and was not readily transferred into either the systemic circulation or cancer cells and tissues. The distribution of paclitaxel into cancer tissues was also low after i.v. administration. Docetaxel was more extensively distributed into cancer tissues than paclitaxel after administration via both routes.

Moreover, we found that i.p. administration of docetaxel rather than i.v. injection was pharmacokinetically superior in the treatment of peritoneal dissemination of cancer in mice [17, 19]. Docetaxel (8 mg/kg) was intravenously or intraperitoneally injected into athymic nude mice with peritoneal dissemination of MKN-45P human gastric cancer, and we measured the concentration changes in plasma, ascitic fluid, solid cancer tissue, and cancer cells suspended in the peritoneal cavity (Figure 6). The drug concentration in ascitic fluid was about 100-fold higher after i.p. injection than after i.v. injection, while the plasma concentrations were rather similar. In suspended free cancer cells in the peritoneal cavity, the drug concentration was much higher in the i.p. group than in the i.v. group, in parallel with the concentrations in ascites after drug injection via these routes. In the case of i.v. injection, the drug appeared rapidly in solid cancer tissue and then the concentration gradually decreased, following the change in the plasma concentration, but the apparent cancer tissue to plasma concentration ratio (Kp,app) was maintained at about 3 to 8 for 8 h, as observed in the AH130-bearing rat model (Figure 5). Docetaxel concentration in solid cancer was maintained at a higher level from 2 h to 8 h after i.p. injection as compared with that after i.v. injection. On the other hand, the docetaxel concentrations in normal organs rapidly decreased up to 1 h and then gradually decreased in the i.v. group, while in the i.p. group the concentrations increased up to 2 or 4 h after injection and then slowly decreased [17]. Namely, docetaxel injected into the peritoneal cavity was transferred rather slowly to the peripheral blood flow; the ratio of AUC_p/AUC_a after i.p. injection of docetaxel was 0.071, but when i.v. injected, the drug passed comparatively easily into the peritoneal cavity from the blood flow; the ratio of AUC_a/AUC_p after i.v. injection was 0.233 although it has been reported the existence of a blood-peritoneal barrier [2]. These results indicate that the i.p. injection of docetaxel was considered to be advantageous as a treatment method for peritoneal dissemination of cancers, offering higher local drug concentration and low systemic toxicity compared with i.v. injection.

4. Influence of Surfactant Vehicles on the Pharmacokinetic Behavior of Taxanes

Because paclitaxel and docetaxel have physicochemically similar properties, the difference of distribution after administration of these drugs may be attributed largely to the surfactant vehicles used to micellize and dissolve these drugs, but not the properties of the drugs themselves. Taxane anticancer drugs are commercially available as micellar preparations, Taxol and Taxotere, which consist of paclitaxel in crEL and docetaxel in PS-80, respectively. It has been reported that surfactants increase cellular accumulation of anticancer drugs and modulate the drug resistance of cancers expressing P-glycoprotein [20, 21]. On the other hand, crEL has been reported to inhibit the intestinal absorption and tissue permeability of paclitaxel [22–25]. However, P-glycoprotein is an efflux transporter in both multidrug-resistant cells and small intestinal epithelium cells, and therefore if these surfactants only inhibit the function of P-glycoprotein, drug accumulation should increase. This apparent contradiction may be explained as follows. CrEL increased the sensitivity of multidrug-resistant cells to daunorubicin at concentrations over 0.1 μL/mL (0.01%) and completely reversed the resistance at 2.0 μL/mL (0.2%) [26, 27]. PS-80 has also been shown to be a multidrug resistance modulator in vitro at concentrations between 0.2 and 0.3 μL/mL (0.02–0.03%) [21, 28] but was ineffective in vivo, because of its very rapid clearance [27, 29]. Then, we examined the influence of crEL and PS-80 on the in vitro uptake of taxanes into AH130 cells, which do not express P-glycoprotein [30]. The intracellular uptake of docetaxel and paclitaxel decreased with increasing vehicle concentration (Figure 7). When these drugs were dissolved in 0.0125% ethanol (final concentration), the intracellular amounts of these drugs were similar, but in the presence of surfactants (at concentrations above 0.0125%) paclitaxel transport into the cells was less than half that of docetaxel. CrEL and PS-80 at concentrations above 0.5% both inhibited paclitaxel entry into red blood cells, in a concentration-dependent manner and with similar potency [18]. These results indicate that both surfactants inhibit the plasma membrane permeability at concentrations above 0.125%, although they can modulate the P-glycoprotein-dependent drug transport at lower concentrations. It is thought that the cell membrane permeability of taxanes is determined by the degree of affinity for, and the ease of dissociation from, surfactant micelles [31]. Paclitaxel seems to be trapped in the surfactant micelles more easily and binds to them more strongly than docetaxel.

Figure 7

Effects of surfactants on uptake of paclitaxel and docetaxel in AH130 cells. Cells were treated with 3 μg/mL of docetaxel (DOC) or paclitaxel (PAC) dissolved with 0.125% ethanol (0) or the indicated concentrations of crEL or PS-80 (PS) for 30 min. The data at 0.0125% concentration of these surfactants are taken from [15]. Each column with bar represents the mean ± SD of at least three experiments performed in triplicate. *,**Significantly different from docetaxel at and 0.01, respectively.

Next, we compared the influence of surfactants on the in vivo pharmacokinetics of taxanes administered intraperitoneally to rats [18]. After injection of paclitaxel in 4.2% crEL into the peritoneal cavity, the permeation of paclitaxel into the systemic circulation was very slow compared with that of docetaxel in 1.5% PS-80. However, the permeation of docetaxel from the peritoneal cavity to the peripheral blood stream was markedly decreased by changing the surfactant from 1.5% PS-80 to 4.2% crEL though it did not reach the level of paclitaxel in 4.2% crEL. van Tellingen et al. [29] noted that PS-80 does not interfere with the disposition kinetics of docetaxel. However, the peritoneal permeability of docetaxel was lowered by increasing the concentration of PS-80 to 7.5% (Table 3).

Thus, the disposition kinetics of paclitaxel is influenced more strongly than that of docetaxel by micellar surfactants, as the concentration is increased.

5. Influence of Surfactants on the Anticancer Effect of Taxanes

Finally, we examined the influence of surfactants on the anticancer effect of docetaxel after i.p. administration to AH130-bearing rats. The anticancer effect of docetaxel became less potent as the concentration of PS-80 was increased (Figure 8). The surfactant not only decreased the permeation of the taxane into the systemic circulation and maintained a high concentration of the drugs in the peritoneal cavity (Table 2), but also inhibited the drug transport into cancer cells, in a concentration-dependent manner, thereby reducing the anticancer effect. Similarly, it is thought that the anticancer effect of paclitaxel is strongly influenced by its vehicle, crEL, because the cell permeation of paclitaxel is readily inhibited by surfactants. The antitumor potency of Taxotere is known to be about 3 times that of Taxol. But, this difference in the potency of these antitumor drugs may be due largely to the difference in the kind and concentration of micellar surfactants used. Moreover, it has been reported that PS-80 is readily degraded by serum esterase [27, 29, 31], while crEL is stable in the body [32]. Consequently, because Taxotere readily releases docetaxel in the peritoneal cavity so that it can rapidly permeate into the systemic circulation, not only can docetaxel be directly transported into cancer cells, but also the drug can be distributed to cancer cells from the blood. This has been called the “sandwich effect” of Taxotere or the dual anticancer effect of docetaxel [33]. Taxol, a paclitaxel formulation with crEL, hardly releases the antitumor agent, so the distribution to tumors is small, and the antitumor potency may be less than that of Taxotere.

6. Conclusion and Perspective

Though the chemical and physical properties of taxane anticancer drugs, paclitaxel, and docetaxel are very similar, the disposition kinetics of these drugs are markedly influenced by their micellar surfactant vehicles after administration of commercial preparations. To treat peritoneal dissemination of cancers, i.p. administration seems logically preferable to systemic administration. In fact, after i.p. administration of commercial preparations diluted with physiological solution, paclitaxel showed a much higher i.p. concentration and less penetration into the systemic circulation than docetaxel. Consequently, the anticancer effect of paclitaxel appears to be stronger than that of docetaxel. However, actually the opposite is the case because the cell permeability of paclitaxel is significantly inhibited by surfactants. Taxol is a micellar formulation of paclitaxel in crEL, of which the content is much higher than in other crEL micellar preparations [34]. Taxotere is a preparation of docetaxel micellized with PS-80, which is rapidly degraded in the body and readily releases the anticancer ingredient, as compared with crEL. These characteristics seem to be the reasons why the anticancer effect of Taxotere is more potent than that of Taxol. Moreover, because many drugs are solubilized in a micellar surfactant vehicle, such as crEL, pharmacokinetic and pharmacodynamic drug-drug interactions may occur when hydrophobic drugs are administered in combination with an injection preparation containing a surfactant vehicle [35]. Further, a preparation not containing crEL is desirable to avoid hypersensitivity reaction. Recently, Abraxane has been developed as a novel crEL-free nanoparticle albumin-bound paclitaxel preparation. Data on the disposition kinetics of paclitaxel after i.p. administration of the preparation have not yet been reported and would be of considerable interest. Furthermore, hyperthermic intraperitoneal chemoperfusion (HIPEC) has been developed for treatment for peritoneal cancers with a variety of anticancer agents. It will also be important to study the pharmacokinetics of anticancer drugs in HIPEC to ensure safe and effective treatment.

Conflict of Interests

The authors do not have any conflict of interests with the content of the manuscript.

References

J. F. Diaz and J. M. Andreu, “Assembly of purified GDP-tubulin into microtubules induced by taxol and taxotere: reversibility, ligand stoichiometry, and competition,” Biochemistry, vol. 32, no. 11, pp. 2747–2755, 1993.
View at: Google Scholar
N. Furui, T. Yamazaki, K. Yokogawa, Y. Fushida, K. Miwa, and K. Miyamoto, “Ascites and the plasma cencentration-time courses of the taxanes after an intraperitoneal administration in patients with peritoneal tumors,” Japanese Journal of Pharmaceutical Health Care and Sciences, vol. 29, no. 3, pp. 263–269, 2003.
View at: Google Scholar
S. Fushida, F. Nao, S. Kinami et al., “Pharmacologic study of intraperitoneal docetaxel in gastric cancer patients with peritoneal dissemination,” Japanese Journal of Cancer and Chemotherapy, vol. 29, no. 10, pp. 1759–1763, 2002.
View at: Google Scholar
S. Fushida, N. Furui, S. Kinami et al., “Pharmacologic study of intraperitoneal paclitaxel in gastric cancer patients with peritoneal dissemination,” Japanese Journal of Cancer and Chemotherapy, vol. 29, no. 12, pp. 2164–2167, 2002.
View at: Google Scholar
Y. Yonemura, E. Bandou, K. Kinoshita et al., “Effective therapy for peritoneal dissemination in gastric cancer,” Surgical Oncology Clinics of North America, vol. 12, no. 3, pp. 635–648, 2003.
View at: Publisher Site | Google Scholar
P. H. Sugarbaker, J. T. Mora, P. Carmignani, O. A. Stuart, and D. Yoo, “Update on chemotherapeutic agents utilized for perioperative intraperitoneal chemotherapy,” Oncologist, vol. 10, no. 2, pp. 112–122, 2005.
View at: Publisher Site | Google Scholar
P. H. Sugarbaker, “Peritoneal-plasma barrier,” in Peritoneal Carcinomatosis: Principles of Management, P. H. Sugarbaker, Ed., pp. 53–63, Kluwer Academic Publisher, Boston, Mass, USA, 1996.
View at: Google Scholar
J. C. Vergniol, R. Bruno, G. Montay, and A. Frydman, “Determination of Taxotere in human plasma by a semi-automated high-performance liquid chromatographic method,” Journal of Chromatography, vol. 582, no. 1-2, pp. 273–278, 1992.
View at: Publisher Site | Google Scholar
W. J. Loos, J. Verweij, K. Nooter, G. Stoter, and A. Sparreboom, “Sensitive determination of docetaxel in human plasma by liquid-liquid extraction and reversed-phase high-performance liquid chromatography,” Journal of Chromatography B, vol. 693, no. 2, pp. 437–441, 1997.
View at: Publisher Site | Google Scholar
F. Mohamed and P. H. Sugarbaker, “Intraperitoneal taxanes,” Surgical Oncology Clinics of North America, vol. 12, no. 3, pp. 825–833, 2003.
View at: Publisher Site | Google Scholar
L. S. Hofstra, A. M. E. Bos, E. G. E. de Vries et al., “Kinetic modeling and efficacy of intraperitoneal paclitaxel combined with intravenous cyclophosphamide and carboplatin as first-line treatment in ovarian cancer,” Gynecologic Oncology, vol. 85, no. 3, pp. 517–523, 2002.
View at: Publisher Site | Google Scholar
F. Mohamed, O. A. Stuart, and P. H. Sugarbaker, “Pharmacokinetics and tissue distribution of intraperitoneal docetaxel with different carrier solutions,” Journal of Surgical Research, vol. 113, no. 1, pp. 114–120, 2003.
View at: Publisher Site | Google Scholar
R. J. Morgan, J. H. Doroshow, T. Synold et al., “Phase I trial of intraperitoneal docetaxel in the treatment of advanced malignancies primarily confined to the peritoneal cavity dose-limiting toxicity and pharmacokinetics,” Clinical Cancer Research, vol. 9, pp. 5896–5901, 2003.
View at: Google Scholar
M. C. Bissery, G. Nohynek, G. Sanderink, and F. Lavelle, “Docetaxel (Taxotere): a review of preclinical and clinical experience. part I: preclinical experience,” Anti-Cancer Drugs, vol. 6, no. 3, pp. 339–368, 1995.
View at: Google Scholar
T. Yoshida, “Contributions of the ascites hepatoma to the concept of malignancy of cancer,” Annals of the New York Academy of Sciences, vol. 63, no. 5, pp. 852–881, 1956.
View at: Google Scholar
Y. Kamijo, C. Ito, M. Nomura, Y. Sai, and K. Miyamoto, “Surfactants influence the distribution of taxanes in peritoneal dissemination tumor-bearing rats,” Cancer Letters, vol. 287, no. 2, pp. 182–186, 2010.
View at: Publisher Site | Google Scholar
Y. Yonemura, Y. Endou, E. Bando et al., “Effect of intraperitoneal administration of docetaxel on peritoneal dissemination of gastric cancer,” Cancer Letters, vol. 210, no. 2, pp. 189–196, 2004.
View at: Publisher Site | Google Scholar
T. Shimada, M. Nomura, K. Yokogawa et al., “Pharmacokinetic advantage of intraperitoneal injection of docetaxel in the treatment for peritoneal dissemination of cancer in mice,” Journal of Pharmacy and Pharmacology, vol. 57, no. 2, pp. 177–181, 2005.
View at: Publisher Site | Google Scholar
G. J. Schuurhuis, H. J. Broxterman, H. M. Pinedo et al., “The polyoxyethylene castor oil Cremophor EL modifies multidrug resistance,” British Journal of Cancer, vol. 62, no. 4, pp. 591–594, 1990.
View at: Google Scholar
E. Friche, P. B. Jensen, M. Sehested, E. J. F. Demant, and N. N. Nissen, “The solvents Cremophor EL and Tween 80 modulate daunorubicin resistance in the multidrug resistant Ehrlich ascites tumor,” Cancer Communications, vol. 2, no. 9, pp. 297–303, 1990.
View at: Google Scholar
A. Sparreboom, O. van Teilingen, W. J. Nooijen, and J. H. Beijnen, “Nonlinear pharmacokinetics of paclitaxel in mice results from the pharmaceutical vehicle cremophor EL,” Cancer Research, vol. 56, no. 9, pp. 2112–2115, 1996.
View at: Google Scholar
A. G. Ellis and L. K. Webster, “Inhibition of paclitaxel elimination in the isolated perfused rat liver by Cremophor EL,” Cancer Chemotherapy and Pharmacology, vol. 43, no. 1, pp. 13–18, 1999.
View at: Publisher Site | Google Scholar
H. A. Bardelmeijer, M. Ouwehand, M. M. Malingre, J. H. Schellens, J. H. Beijnen, and O. van Tellingen, “Entrapment by Cremophor EL decreases the absorption of paclitaxel from the gut,” Cancer Chemotherapy and Pharmacology, vol. 49, no. 2, pp. 119–125, 2002.
View at: Publisher Site | Google Scholar
H. Gelderblom, J. Verweij, D. M. van Zomeren et al., “Influence of Cremophor EL on the bioavailability of intraperitoneal paclitaxel,” Clinical Cancer Research, vol. 8, no. 4, pp. 1237–1241, 2002.
View at: Google Scholar
L. K. Webster, M. E. Linsenmeyer, M. J. Millward, C. Morton, J. F. Bishop, and D. M. Woodcock, “Measurement of cremophor EL following taxol: plasma levels sufficient to reverse drug exclusion mediated by the multidrug-resistant phenotype,” Journal of the National Cancer Institute, vol. 85, no. 20, pp. 1685–1690, 1993.
View at: Google Scholar
L. K. Webster, M. E. Linsenmeyer, D. Rischin, M. E. Urch, D. M. Woodcock, and M. J. Millward, “Plasma concentrations of polysorbate 80 measured in patients following administration of docetaxel or etoposide,” Cancer Chemotherapy and Pharmacology, vol. 39, no. 6, pp. 557–560, 1997.
View at: Publisher Site | Google Scholar
D. M. Woodcock, M. E. Linsenmeyer, G. Chojnowski et al., “Reversal of multidrug resistance by surfactants,” British Journal of Cancer, vol. 66, no. 1, pp. 62–68, 1992.
View at: Google Scholar
O. van Tellingen, J. H. Beijnen, J. Verweij, E. J. Scherrenburg, W. J. Nooijen, and A. Sparreboom, “Rapid esterase-sensitive breakdown of polysorbate 80 and its impact on the plasma pharmacokinetics of docetaxel and metabolites in mice,” Clinical Cancer Research, vol. 5, no. 10, pp. 2918–2924, 1999.
View at: Google Scholar
S. Wakusawa, S. Nakamura, and K. Miyamoto, “Establishment by adriamycin exposure of multidrug-resistant rat ascites hepatoma AH130 cells showing low DT-diaphorase activity and high cross resistance to mitomycins,” Japanese Journal of Cancer Research, vol. 88, no. 1, pp. 88–96, 1997.
View at: Google Scholar
K. Yokogawa, M. Jin, N. Furui et al., “Disposition kinetics of taxanes after intraperitoneal administration in rats and influence of surfactant vehicles,” Journal of Pharmacy and Pharmacology, vol. 56, no. 5, pp. 629–634, 2004.
View at: Publisher Site | Google Scholar
L. van Zuylen, J. Verweij, and A. Sparreboom, “Role of formulation vehicles in taxane pharmacology,” Investigational New Drugs, vol. 19, no. 2, pp. 125–141, 2001.
View at: Publisher Site | Google Scholar
A. Sparreboom, J. Verweij, M. E. L. van de Burg et al., “Disposition of Cremophor EL in humans limits the potential for modulation of the multidrug resistance phenotype in vivo,” Clinical Cancer Research, vol. 4, no. 8, pp. 1937–1942, 1998.
View at: Google Scholar
S. Fushida, J. Kinoshita, Y. Yagi et al., “Dual anti-cancer effects of weekly intraperitoneal docetaxel in treatment of advanced gastric cancer patients with peritoneal carcinomatosis: a feasibility and pharmacokinetic study,” Oncology Reports, vol. 19, no. 5, pp. 1305–1310, 2008.
View at: Google Scholar
R. T. Dorr, “Pharmacology and toxicology of Cremophor EL diluent,” Annals of Pharmacotherapy, vol. 28, no. 5, pp. S11–S14, 1994.
View at: Google Scholar
M. Jin, T. Shimada, K. Yokogawa et al., “Cremophor EL releases cyclosporin A adsorbed on blood cells and blood vessels, and increases apparent plasma concentration of cyclosporin A,” International Journal of Pharmaceutics, vol. 293, no. 1-2, pp. 137–144, 2005.
View at: Publisher Site | Google Scholar

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Copyright © 2012 Ken'ichi Miyamoto 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.

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