Cremophor EL: the drawbacks and advantages of vehicle selection for drug formulation.

Cremophor EL (CrEL) is a formulation vehicle used for various poorly-water soluble drugs, including the anticancer agent paclitaxel (Taxol). In contrast to earlier reports, CrEL is not an inert vehicle, but exerts a range of biological effects, some of which have important clinical implications. Its use has been associated with severe anaphylactoid hypersensitivity reactions, hyperlipidaemia, abnormal lipoprotein patterns, aggregation of erythrocytes and peripheral neuropathy. The pharmacokinetic behaviour of CrEL is dose-independent, although its clearance is highly influenced by duration of the infusion. This is particularly important since CrEL can affect the disposition of various drugs by changing the unbound drug concentration through micellar encapsulation. In addition, it has been shown that CrEL, as an integral component of paclitaxel chemotherapy, modifies the toxicity profile of certain anticancer agents given concomitantly, by mechanisms other than kinetic interference. A clear understanding of the biological and pharmacological role of CrEL is essential to help oncologists avoid side-effects associated with the use of paclitaxel or other agents using this vehicle. With the present development of various new anticancer agents, it is recommended that alternative formulation approaches should be pursued to allow a better control of the toxicity of the treatment and the pharmacological interactions related to the use of CrEL.

[1]  J. Barré,et al.  Problems in therapeutic drug monitoring: free drug level monitoring. , 1988, Therapeutic drug monitoring.

[2]  N. Gleicher,et al.  Cytotoxic effects of free fatty acids on ascites tumor cells. , 1987, Journal of the National Cancer Institute.

[3]  J. Verweij,et al.  Quantitation of Cremophor EL in human plasma samples using a colorimetric dye-binding microassay. , 1998, Analytical biochemistry.

[4]  A. G. Ellis,et al.  Inhibition of paclitaxel elimination in the isolated perfused rat liver by Cremophor EL , 1999, Cancer Chemotherapy and Pharmacology.

[5]  S. Brimijoin,et al.  Emulsifier for intravenous cyclosporin inhibits neurite outgrowth, causes deficits in rapid axonal transport and leads to structural abnormalities in differentiating N1E.115 neuroblastoma. , 1992, The Journal of pharmacology and experimental therapeutics.

[6]  J. Verweij,et al.  Paclitaxel (Taxol) and docetaxel (Taxotere): not simply two of a kind. , 1994, Annals of oncology : official journal of the European Society for Medical Oncology.

[7]  G. Forbes,et al.  Central Nervous System Toxicity after Liver Transplantation , 1987 .

[8]  J. Bergh,et al.  Is Cremophor EL, solvent for paclitaxel, cytotoxic? , 1993, The Lancet.

[9]  Mark L. Greenberg,et al.  Anaphylactoid reactions in children receiving high-dose intravenous cyclosporine for reversal of tumor resistance: the causative role of improper dissolution of Cremophor EL. , 1995, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[10]  G. Giaccone,et al.  Pharmacokinetics of paclitaxel and carboplatin in a dose-escalating and dose-sequencing study in patients with non-small-cell lung cancer. The European Cancer Centre. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  G. Bonadonna,et al.  Human pharmacokinetic characterization and in vitro study of the interaction between doxorubicin and paclitaxel in patients with breast cancer. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[12]  F. Hamada,et al.  Differential alteration of cisplatin cytotoxicity and myelotoxicity by the paclitaxel vehicle cremophor EL , 2000, Naunyn-Schmiedeberg's Archives of Pharmacology.

[13]  J. Verweij,et al.  Differential modulation of cisplatin accumulation in leukocytes and tumor cell lines by the paclitaxel vehicle Cremophor EL. , 1997, Annals of oncology : official journal of the European Society for Medical Oncology.

[14]  M. Millward,et al.  Measurement of cremophor EL following taxol: plasma levels sufficient to reverse drug exclusion mediated by the multidrug-resistant phenotype. , 1993, Journal of the National Cancer Institute.

[15]  A. Weinstein,et al.  Unusual serum lipoprotein abnormality induced by the vehicle of miconazole. , 1977, The New England journal of medicine.

[16]  J. Bergh,et al.  The cytotoxic activity of Taxol in primary cultures of tumour cells from patients is partly mediated by Cremophor EL. , 1995, British Journal of Cancer.

[17]  R S Weinstein,et al.  Solutol HS 15, nontoxic polyoxyethylene esters of 12-hydroxystearic acid, reverses multidrug resistance. , 1991, Cancer research.

[18]  J B Vermorken,et al.  European-Canadian randomized trial of paclitaxel in relapsed ovarian cancer: high-dose versus low-dose and long versus short infusion. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[19]  V. Ling,et al.  Effects of nonionic detergents on P-glycoprotein drug binding and reversal of multidrug resistance. , 1993, Cancer research.

[20]  B. Williams,et al.  Reversal of the multidrug resistance phenotype with cremophor EL, a common vehicle for water-insoluble vitamins and drugs. , 1990, Cancer research.

[21]  W. Sawyer,et al.  Reversal of multidrug resistance by surfactants. , 1992, British journal of cancer.

[22]  J Verweij,et al.  Cremophor EL-mediated alteration of paclitaxel distribution in human blood: clinical pharmacokinetic implications. , 1999, Cancer research.

[23]  A. Windebank,et al.  Potential neurotoxicity of the solvent vehicle for cyclosporine. , 1994, The Journal of pharmacology and experimental therapeutics.

[24]  J. Böhler,et al.  Titrimetric determination of Cremophor EL in aqueous solutions and biofluids: part 2: ruggedness of the method with respect to biofluids. , 1999, Journal of pharmaceutical and biomedical analysis.

[25]  J Verweij,et al.  Inter-relationships of paclitaxel disposition, infusion duration and Cremophor EL kinetics in cancer patients , 2000, Anti-cancer drugs.

[26]  B. Leyland-Jones,et al.  Hypersensitivity reactions from taxol. , 1990, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[27]  D. Kessel,et al.  Effects of Cremophor EL on distribution of Taxol to serum lipoproteins. , 1994, British Journal of Cancer.

[28]  J. Verweij,et al.  Docetaxel and paclitaxel inhibit DNA-adduct formation and intracellular accumulation of cisplatin in human leukocytes , 1996, Cancer Chemotherapy and Pharmacology.

[29]  J. W. Wilson,et al.  Taxol: a history of pharmaceutical development and current pharmaceutical concerns. , 1993, Journal of the National Cancer Institute. Monographs.

[30]  J. Beijnen,et al.  Determination of polyoxyethyleneglycerol triricinoleate 35 (Cremophor EL) in plasma by pre-column derivatization and reversed-phase high-performance liquid chromatography. , 1996, Journal of chromatography. B, Biomedical applications.

[31]  G. Volcheck,et al.  Anaphylaxis to intravenous cyclosporine and tolerance to oral cyclosporine: case report and review. , 1998, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[32]  J. Beijnen,et al.  Nonlinear pharmacokinetics of paclitaxel in mice results from the pharmaceutical vehicle Cremophor EL. , 1996, Cancer research.

[33]  J. B. Vermorken,et al.  The polyoxyethylene castor oil Cremophor EL modifies multidrug resistance. , 1990, British Journal of Cancer.

[34]  D. Kessel,et al.  Fractionation of Cremophor EL delineates components responsible for plasma lipoprotein alterations and multidrug resistance reversal. , 1995, Oncology research.

[35]  D. Horrobin,et al.  Polyunsaturated fatty acid-induced cytotoxicity against tumor cells and its relationship to lipid peroxidation. , 1988, Journal of the National Cancer Institute.

[36]  H. Pinedo Development of new anti-cancer drugs , 1986, Medical oncology and tumor pharmacotherapy.

[37]  A. McPhail,et al.  Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. , 1971, Journal of the American Chemical Society.

[38]  D. Kessel,et al.  The alteration of plasma lipoproteins by cremophor EL. , 1994, Journal of photochemistry and photobiology. B, Biology.

[39]  J. Beijnen,et al.  Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[40]  P. Sonneveld,et al.  Clinical relevance of P-glycoprotein expression in haematological malignancies. , 1994, Leukemia research.

[41]  M. Millward,et al.  Cremophor pharmacokinetics in patients receiving 3-, 6-, and 24-hour infusions of paclitaxel. , 1996, Journal of the National Cancer Institute.

[42]  J. Kigawa,et al.  Effects of Taxol on blood cells , 1998, The Lancet.

[43]  B. Williams,et al.  Haematopoietic radioprotection by Cremophor EL: a polyethoxylated castor oil. , 1995, International journal of radiation biology.

[44]  R. Larsson,et al.  Differential activity of cremophor EL and paclitaxel in patients' tumor cells and human carcinoma cell lines in vitro , 1997, Cancer.

[45]  F M Muggia,et al.  Complement activation by Cremophor EL as a possible contributor to hypersensitivity to paclitaxel: an in vitro study. , 1998, Journal of the National Cancer Institute.

[46]  J. Verweij,et al.  Measurement of fraction unbound paclitaxel in human plasma. , 2000, Drug metabolism and disposition: the biological fate of chemicals.

[47]  D M Woodcock,et al.  Phase I trial of cremophor EL with bolus doxorubicin. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.

[48]  J. L. Biedler,et al.  Potentiation of drug effect by Tween 80 in Chinese hamster cells resistant to actinomycin D and daunomycin. , 1972, Cancer research.

[49]  G. Giaccone,et al.  Cremophor EL pharmacokinetics in a phase I study of paclitaxel (Taxol®) and carboplatin in non-small cell lung cancer patients , 2000, Anti-cancer drugs.

[50]  E K Rowinsky,et al.  Cardiac disturbances during the administration of taxol. , 1991, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[51]  J. Verweij,et al.  Linearized colorimetric assay for cremophor EL: application to pharmacokinetics after 1-hour paclitaxel infusions. , 1998, Analytical biochemistry.

[52]  J. Watkins,et al.  Adverse reactions to intravenous anaesthetic induction agents. , 1977, British medical journal.

[53]  M. Sehested,et al.  The solvents cremophor EL and Tween 80 modulate daunorubicin resistance in the multidrug resistant Ehrlich ascites tumor. , 1990, Cancer communications.

[54]  G. Hortobagyi,et al.  Sequence-dependent alteration of doxorubicin pharmacokinetics by paclitaxel in a phase I study of paclitaxel and doxorubicin in patients with metastatic breast cancer. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[55]  E K Rowinsky,et al.  Sequences of taxol and cisplatin: a phase I and pharmacologic study. , 1991, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[56]  J. Verweij,et al.  Disposition of [G-(3)H]paclitaxel and cremophor EL in a patient with severely impaired renal function. , 1999, Drug metabolism and disposition: the biological fate of chemicals.

[57]  E. Eisenhauer,et al.  Clinical toxicities encountered with paclitaxel (Taxol). , 1993, Seminars in oncology.

[58]  J. Beijnen,et al.  Pharmaceutical Development of (Investigational) Anticancer Agents for Parenteral Use-A Review , 1996 .

[59]  A. Olesen,et al.  Complement-mediated reactions to diazepam with Cremophor as solvent (Stesolid MR). , 1980, British journal of anaesthesia.

[60]  J Moan,et al.  Interaction of cremophor EL with human plasma. , 1991, International Journal of Biochemistry.

[61]  J. Verweij,et al.  Disposition of Cremophor EL in humans limits the potential for modulation of the multidrug resistance phenotype in vivo. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.

[62]  M. Brecher,et al.  Cremophor-EL enhances taxol efficacy in a multi-drug resistant C1300 neuroblastoma cell line. , 1993, Anticancer research.

[63]  Takashi Tsuruo,et al.  Cremophor EL reversed multidrug resistance in vitro but not in tumor-bearing mouse models , 1996, Anti-cancer drugs.

[64]  E. Warner,et al.  Patient preferences for oral versus intravenous palliative chemotherapy. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[65]  J. Verweij,et al.  Rapid esterase-sensitive breakdown of polysorbate 80 and its impact on the plasma pharmacokinetics of docetaxel and metabolites in mice. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.

[66]  K. Osann,et al.  Comparison of cyclosporin A, verapamil, PSC-833 and cremophor EL as enhancing agents of VP-16 in murine lymphoid leukemias. , 1995, Leukemia research.