References
- Bae, Y., Diezi, T.A., Zhao, A., Kwon, G.S. (2007). Mixed polymeric micelles for combination cancer chemotherapy through the concurrent delivery of multiple chemotherapeutic agents. J Contr Rel. 122:324–30.
- Chen, H., Wang, Y., Xu, J., Ji, J., Zhang, J., Hu, Y., Gu, Y. (2008). Non-invasive near infrared fluorescence imaging of CdHgTe quantum dots in mouse model. J Fluoresc. 18:801–11.
- Cho, Y.W., Park, S.A., Han, T.H., Son, D.H., Park, J.S., Oh, S.J., Moon, D.H., Cho, K.J., Ahn, C.H., Byun, Y., Kim, I.S., Kwon, I.C., Kim, S.Y. (2007). In vivo tumor targeting and radionuclide imaging with self-assembled nanoparticles: mechanisms, key factors, and their implications. Biomaterials. 28:1236–47.
- Crosasso, P., Ceruti, M., Brusa, P., Arpicco, S., Dosio, F., Cattel, L. (2000). Preparation, characterization and properties of sterically stabilized paclitaxel-containing liposomes. J Contr Rel. 63:19–30.
- Danson, S., Ferry, D., Alakhov, V., Margison, J., Kerr, D., Jowle, D., Brampton, M., Halbert, G., Ranson, M. (2004). Phase I dose escalation and pharmacokinetic study of pluronic polymer-bound doxorubicin (SP1049C) in patients with advanced cancer. Br J Cancer. 90;2085–91.
- Desai, N., Trieu, V., Yao, Z., Louie, L., Ci, S., Yang, A., Tao, C., De, T., Beals, B., Dykes, D., Noker, P., Yao, R., Labao, E., Hawkins, M., Soon-Shiong, P. (2006). Increased antitumor activity, intratumor paclitaxel concentrations, and endothelial cell transport of cremophor-free, albumin-bound paclitaxel, ABI-007, compared with cremophor-based paclitaxel. Clin Cancer Res. 12:1317–24.
- Dhanikula, A.B., Singh, D.R., Panchagnula, R. (2005). In vivo pharmacokinetic and tissue distribution studies in mice of alternative formulations for local and systemic delivery of Paclitaxel: gel, film, prodrug, liposomes and micelles. Curr Drug Deliv. 2:35–44.
- Hruby, M., Konak, C., Ulbrich, K. (2005). Polymeric micellar pH-sensitive drug delivery system for doxorubicin. J Contr Rel. 103:137–48.
- Huh, K.M., Lee, S.C., Cho, Y.W., Lee, J., Jeong, J.H., Park, K. (2005). Hydrotropic polymer micelle system for delivery of paclitaxel. J Contr Rel. 101:59–68.
- Huh, K.M., Min, H.S., Lee, S.C., Lee, H.J., Kim, S., Park, K. (2008). A new hydrotropic block copolymer micelle system for aqueous solubilization of paclitaxel. J Contr Rel. 126:122–9.
- Huo, M., Zhang, Y., Zhou, J., Zou, A., Yu, D., Wu, Y., Li, J., Li, H. (2010). Synthesis and characterization of low-toxic amphiphilic chitosan derivatives and their application as micelle carrier for antitumor drug. Int J Pharmaceut. 394:162–73.
- Ibrahim, N.K., Desai, N., Legha, S., Soon-Shiong, P., Theriault, R.L., Rivera, E., Esmaeli, B., Ring, S.E., Bedikian, A., Hortobagyi, G.N., Ellerhorst, J.A. (2002). Phase I and pharmacokinetic study of ABI-007, a Cremophor-free, protein-stabilized, nanoparticle formulation of paclitaxel. Clin Cancer Res. 8:1038–44.
- Ibrahim, N.K., Samuels, B., Page, R., Doval, D., Patel, K.M., Rao, S.C., Nair, M.K., Bhar, P., Desai, N., Hortobagyi, G.N. (2005). Multicenter phase II trial of ABI-007, an albumin-bound paclitaxel, in women with metastatic breast cancer. J Clin Oncol. 23:6019–26.
- Kim, S.C., Kim, D.W., Shim, Y.H., Bang, J.S., Oh, H.S., Wan Kim, S., Seo, M.H. (2001). In vivo evaluation of polymeric micellar paclitaxel formulation: toxicity and efficacy. J Contr Rel. 72:191–202.
- Kwon, G.S. (2003). Polymeric micelles for delivery of poorly water-soluble compounds. Crit Rev Ther Drug Carrier Syst. 20:357–3.
- Kwon, G.S., Yokoyama, M., Okano, T., Sakurai, Y., Kataoka, K. (1993). Biodistribution of micelle-forming polymer-drug conjugates. Pharm Res. 10:970–4.
- Lee, A.L., Wang, Y., Cheng, H.Y., Pervaiz, S., Yang, Y.Y. (2009). The co-delivery of paclitaxel and Herceptin using cationic micellar nanoparticles. Biomaterials. 30:919–27.
- Lee, E.S., Gao, Z., Kim, D., Park, K., Kwon, I.C., Bae, Y.H. (2008). Super pH-sensitive multifunctional polymeric micelle for tumor pH(e) specific TAT exposure and multidrug resistance. J Contr Rel. 129:228–36.
- Li, H., Liu, J., Ding, S., Zhang, C., Shen, W., You, Q. (2009). Synthesis of novel pH-sensitive chitosan graft copolymers and micellar solubilization of paclitaxel. Int J Biol Macromol. 44:249–56.
- Liggins, R.T., Burt, H.M. (2004). Paclitaxel-loaded poly(L-lactic acid) microspheres 3: blending low and high molecular weight polymers to control morphology and drug release. Int J Pharm. 282:61–71.
- Liu, J., Li, H., Jiang, X., Zhang, C., Ping, Q. (2010). Novel pH-sensitive chitosan-derived micelles loaded with paclitaxel. Carbohydr Polym. 82:432–9.
- Matsumoto, J., Nakada, Y., Sakurai, K., Nakamura, T., Takahashi, Y. (1999). Preparation of nanoparticles consisted of poly(L-lactide)-poly(ethylene glycol)-poly(L-lactide) and their evaluation in vitro. Int J Pharm. 185:93–101.
- Matsumura, Y., Hamaguchi, T., Ura, T., Muro, K., Yamada, Y., Shimada, Y., Shirao, K., Okusaka, T., Ueno, H., Ikeda, M., Watanabe, N. (2004). Phase I clinical trial and pharmacokinetic evaluation of NK911, a micelle-encapsulated doxorubicin. Br J Cancer. 91:1775–81.
- Mizumura, Y., Matsumura, Y., Yokoyama, M., Okano, T., Kawaguchi, T., Moriyasu, F., Kakizoe, T. (2002). Incorporation of the anticancer agent KRN5500 into polymeric micelles diminishes the pulmonary toxicity. Jpn J Cancer Res. 93:1237–43.
- Ooya, T., Lee, J., Park, K. (2003). Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel. J Contr Rel. 93:121–7.
- Qu, G., Yao, Z., Zhang, C., Wu, X., Ping, Q. (2009). PEG conjugated N-octyl-O-sulfate chitosan micelles for delivery of paclitaxel: in vitro characterization and in vivo evaluation. Eur J Pharm Sci. 37:98–105.
- Rapoport, N. (2007). Physical stimuli-responsive polymeric micelles foranti-cancer drug delivery. Prog Polym Sci. 32:962–90.
- Rowinsky, E.K., Donehower, R.C. (1993). The clinical pharmacology of paclitaxel (Taxol). Semin Oncol. 2016–25.
- Sawant, R.R., Torchilin, V.P. (2009). Enhanced cytotoxicity of TATp-bearing paclitaxel-loaded micelles in vitro and in vivo. Int J Pharm. 374:114–8.
- Sawant, R.R., Vaze, O., Rockwell, K., Torchilin, V.P. (2010). Palmitoyl ascorbate-modified liposomes as nanoparticle platform for ascorbate-mediated cytotoxicity and paclitaxel co-delivery. Eur J Pharm Biopharm. 75:321–326.
- Sonnichsen, D.S., Relling, M.V. (1994). Clinical pharmacokinetics of paclitaxel. Clin Pharmacokinet. 27:256–69.
- Spencer, C.M., Faulds, D. (1994). Paclitaxel. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the treatment of cancer. Drugs. 48:794–847.
- Szebeni, J., Muggia, F.M., Alving, C.R. (1998). Complement activation by Cremophor EL as a possible contributor to hypersensitivity to paclitaxel: an in vitro study. J Natl Cancer Inst. 90:300–6.
- Torchilin, V. (2010). Tumor delivery of macromolecular drugs based on the EPR effect. Adv Drug Deliv Rev. (In press).
- Torchilin, V.P. (2001). Structure and design of polymeric surfactant-based drug delivery systems. J Contr Rel. 73:137–72.
- Torchilin, V.P. (2007). Micellar nanocarriers: pharmaceutical perspectives. Pharm Res. 24:1–16.
- van Zuylen, L., Karlsson, M.O., Verweij, J., Brouwer, E., de Bruijn, P., Nooter, K., Stoter, G., Sparreboom, A. (2001). Pharmacokinetic modeling of paclitaxel encapsulation in Cremophor EL micelles. Cancer Chemother Pharmacol. 47:309–18.
- Wanjun, T., Cunxin, W., Donghua, C. (2005). Kinetic studies on the pyrolysis of chitin and chitosan. Polymer Degr Stab. 87:389–94.
- Xie, Z., Guan, H., Chen, X., Lu, C., Chen, L., Hu, X., Shi, Q., Jing, X. (2007). A novel polymer-paclitaxel conjugate based on amphiphilic triblock copolymer. J Contr Rel. 117:210–6.
- Yang, T., Choi, M.K., Cui, F.D., Kim, J.S., Chung, S.J., Shim, C.K., Kim, D.D. (2007). Preparation and evaluation of paclitaxel-loaded PEGylated immunoliposome. J Contr Rel. 120:169–77.
- Yokoyama, M., Miyauchi, M., Yamada, N., Okano, T., Sakurai, Y., Kataoka, K., Inoue, S. (1990). Characterization and anticancer activity of the micelle-forming polymeric anticancer drug adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer. Cancer Res. 50:1693–700.
- Yokoyama, M., Okano, T., Sakurai, Y., Ekimoto, H., Shibazaki, C., Kataoka, K. (1991). Toxicity and antitumor activity against solid tumors of micelle-forming polymeric anticancer drug and its extremely long circulation in blood. Cancer Res. 51:3229–36.
- Zhang, C., Ping, Q., Zhang, H., Jian, S. (2003). Preparation of N-alkyl-O-sulfate chitosan derivatives and micellar solubilization of taxol. Carbohydr Polymers. 54:137–44.
- Zhang, C., Qu, G., Sun, Y., Wu, X., Yao, Z., Guo, Q., Ding, Q., Yuan, S., Shen, Z., Ping, Q., Zhou, H. (2008a). Pharmacokinetics, biodistribution, efficacy and safety of N-octyl-O-sulfate chitosan micelles loaded with paclitaxel. Biomaterials. 29:1233–41.
- Zhang, C., Qu, G., Sun, Y., Yang, T., Yao, Z., Shen, W., Shen, Z., Ding, Q., Zhou, H., Ping, Q. (2008b). Biological evaluation of N-octyl-O-sulfate chitosan as a new nano-carrier of intravenous drugs. Eur J Pharm Sci. 33:415–23.
- Zhang, J., Chen, H., Xu, L., Gu, Y. (2008c). The targeted behavior of thermally responsive nanohydrogel evaluated by NIR system in mouse model. J Contr Rel. 131:34–40.
- Zhang, Y., Tang, L., Sun, L., Bao, J., Song, C., Huang, L., Liu, K., Tian, Y., Tian, G., Li, Z., Sun, H., Mei, L. (2010). A novel paclitaxel-loaded poly(epsilon-caprolactone)/Poloxamer 188 blend nanoparticle overcoming multidrug resistance for cancer treatment. Acta Biomater. 6:2045–52.
- Zhang, Z., Feng, S.S. (2006). The drug encapsulation efficiency, in vitro drug release, cellular uptake and cytotoxicity of paclitaxel-loaded poly(lactide)-tocopheryl polyethylene glycol succinate nanoparticles. Biomaterials. 27:4025–33.
- Zhu, C., Jung, S., Luo, S., Meng, F., Zhu, X., Park, T.G., Zhong, Z. (2010). Co-delivery of siRNA and paclitaxel into cancer cells by biodegradable cationic micelles based on PDMAEMA-PCL-PDMAEMA triblock copolymers. Biomaterials. 31:2408–16.