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Volumn 28, Issue 2, 2013, Pages 298-307

Nanoformulation of paclitaxel to enhance cancer therapy

Author keywords

cancer chemotherapy; drug delivery; nanoformulation; Paclitaxel; pluronic copolymer; water soluble

Indexed keywords

CANCER CHEMOTHERAPY; NANOFORMULATION; PACLITAXEL; PLURONIC COPOLYMERS; WATER-SOLUBLE;

EID: 84881125656     PISSN: 08853282     EISSN: 15308022     Source Type: Journal    
DOI: 10.1177/0885328212446822     Document Type: Article
Times cited : (23)

References (30)
  • 1
    • 41949100244 scopus 로고    scopus 로고
    • Drug nanoparticles: Formulating poorly water-soluble compounds
    • Elaine M, Gary G. Drug nanoparticles: formulating poorly water-soluble compounds. Toxicol Pathol. 2008 ; 36: 43-48
    • (2008) Toxicol Pathol , vol.36 , pp. 43-48
    • Elaine, M.1    Gary, G.2
  • 3
    • 51649088789 scopus 로고    scopus 로고
    • Paclitaxel encapsulated in cationic liposomes increases tumor microvessel leakiness and improves therapeutic efficacy in combination with Cisplatin
    • Strieth S, Eichhorn ME, Werner A, et al. Paclitaxel encapsulated in cationic liposomes increases tumor microvessel leakiness and improves therapeutic efficacy in combination with Cisplatin. Clin Cancer Res. 2008 ; 14: 4603-4611
    • (2008) Clin Cancer Res , vol.14 , pp. 4603-4611
    • Strieth, S.1    Eichhorn, M.E.2    Werner, A.3
  • 4
    • 0033964804 scopus 로고    scopus 로고
    • Preparation, characterization and properties of sterically stabilized paclitaxel-containing liposomes
    • Crosasso P, Ceruti M, Brusa P, et al. Preparation, characterization and properties of sterically stabilized paclitaxel-containing liposomes. J Control Release. 2000 ; 63: 19-30
    • (2000) J Control Release , vol.63 , pp. 19-30
    • Crosasso, P.1    Ceruti, M.2    Brusa, P.3
  • 5
    • 80051711290 scopus 로고    scopus 로고
    • A liposomal formulation able to incorporate a high content of paclitaxel and exert promising anticancer effect
    • Kan P, Tsao CW, Wang AJ, et al. A liposomal formulation able to incorporate a high content of paclitaxel and exert promising anticancer effect. J Drug Deliv. 2011 ; 2011: 1-9
    • (2011) J Drug Deliv , vol.2011 , pp. 1-9
    • Kan, P.1    Tsao, C.W.2    Wang, A.J.3
  • 6
    • 77955262023 scopus 로고    scopus 로고
    • Paclitaxel-loaded polymeric micelles modified with MCF-7 cell-specific phage protein: Enhanced binding to target cancer cells and increased cytotoxicity
    • Wang T, Petrenko VA, Torchilin VP. Paclitaxel-loaded polymeric micelles modified with MCF-7 cell-specific phage protein: enhanced binding to target cancer cells and increased cytotoxicity. Mol Pharm. 2010 ; 7(4): 1007-1014
    • (2010) Mol Pharm , vol.74 , pp. 1007-1014
    • Wang, T.1    Petrenko, V.A.2    Torchilin, V.P.3
  • 7
    • 76749138904 scopus 로고    scopus 로고
    • The formulation of aptamer-coated paclitaxel-polylactide nanoconjugates and their targeting to cancer cells
    • Tong R, Yala L, Fan TM, et al. The formulation of aptamer-coated paclitaxel-polylactide nanoconjugates and their targeting to cancer cells. Biomaterials. 2010 ; 31: 3043-3053
    • (2010) Biomaterials , vol.31 , pp. 3043-3053
    • Tong, R.1    Yala, L.2    Fan, T.M.3
  • 8
    • 77349116167 scopus 로고    scopus 로고
    • Paclitaxel-loaded poly(N-vinylpyrrolidone)-b-poly(epsilon-caprolactone) nanoparticles: Preparation and antitumor activity in vivo
    • Zhu ZS, Li Y, Li XL, et al. Paclitaxel-loaded poly(N-vinylpyrrolidone)-b- poly(epsilon-caprolactone) nanoparticles: preparation and antitumor activity in vivo. J Control Release. 2010 ; 142: 438-446
    • (2010) J Control Release , vol.142 , pp. 438-446
    • Zhu, Z.S.1    Li, Y.2    Li, X.L.3
  • 9
    • 0032828963 scopus 로고    scopus 로고
    • Development of copolymers of poly(d,l-lactide) and methoxypolyethylene glycol as micellar carriers of paclitaxel
    • Burt HM, Zhang XC, Toleikis P, et al. Development of copolymers of poly(d,l-lactide) and methoxypolyethylene glycol as micellar carriers of paclitaxel. Colloids Surf B: Biointerfaces. 1999 ; 16: 161-171
    • (1999) Colloids Surf B: Biointerfaces , vol.16 , pp. 161-171
    • Burt, H.M.1    Zhang, X.C.2    Toleikis, P.3
  • 10
    • 0034032145 scopus 로고    scopus 로고
    • Preparation and characterization of solid lipid nanospheres containing paclitaxel
    • Cavalli R, Caputo O, Gasco MR. Preparation and characterization of solid lipid nanospheres containing paclitaxel. Eur J Pharm Sci. 2000 ; 10: 305-309
    • (2000) Eur J Pharm Sci , vol.10 , pp. 305-309
    • Cavalli, R.1    Caputo, O.2    Gasco, M.R.3
  • 11
    • 33847318019 scopus 로고    scopus 로고
    • Oil-encapsulating PEO-PPO-PEO/PEG shell cross-linked nanocapsules for target-specific delivery of paclitaxel
    • Lee H, Jeong YH, Park TG. Oil-encapsulating PEO-PPO-PEO/PEG shell cross-linked nanocapsules for target-specific delivery of paclitaxel. Biomacromolecules. 2007 ; 8: 650-656
    • (2007) Biomacromolecules , vol.8 , pp. 650-656
    • Lee, H.1    Jeong, Y.H.2    Park, T.G.3
  • 12
    • 34648831611 scopus 로고    scopus 로고
    • In vivo evaluation of lipid nanocapsules as a promising colloidal carrier for paclitaxel
    • Lacoeuille F, Hindre F, Moalc F, et al. In vivo evaluation of lipid nanocapsules as a promising colloidal carrier for paclitaxel. Int J Pharm. 2007 ; 344: 143-149
    • (2007) Int J Pharm , vol.344 , pp. 143-149
    • Lacoeuille, F.1    Hindre, F.2    Moalc, F.3
  • 13
    • 36549018670 scopus 로고    scopus 로고
    • Safety and efficacy of amphiphilic ß-cyclodextrin nanoparticles for paclitaxel delivery
    • Bilensoy E, Gurkaynak O, Dogan AL, et al. Safety and efficacy of amphiphilic ß-cyclodextrin nanoparticles for paclitaxel delivery. Int J Pharm. 2008 ; 347: 163-170
    • (2008) Int J Pharm , vol.347 , pp. 163-170
    • Bilensoy, E.1    Gurkaynak, O.2    Dogan, A.L.3
  • 14
    • 0036554742 scopus 로고    scopus 로고
    • Influence of cremophor El on the bioavailability of intraperitoneal paclitaxel
    • Gelderblom H, Verweij J, Zomeren DM, et al. Influence of cremophor El on the bioavailability of intraperitoneal paclitaxel. Clin Cancer Res. 2002 ; 8: 1237-1241
    • (2002) Clin Cancer Res , vol.8 , pp. 1237-1241
    • Gelderblom, H.1    Verweij, J.2    Zomeren, D.M.3
  • 15
    • 9944229543 scopus 로고    scopus 로고
    • Targeted polymeric micelles for delivery of poorly soluble drugs
    • Torchilin VP. Targeted polymeric micelles for delivery of poorly soluble drugs. Cell Mol Life Sci. 2004 ; 61: 2549-2559
    • (2004) Cell Mol Life Sci , vol.61 , pp. 2549-2559
    • Torchilin, V.P.1
  • 16
    • 72449134369 scopus 로고    scopus 로고
    • Cyclodextrin-based polymeric materials: Synthesis, properties, and pharmaceutical/biomedical applications
    • Manakker F, Vermonden T, Nostrum CF, et al. Cyclodextrin-based polymeric materials: synthesis, properties, and pharmaceutical/biomedical applications. Biomacromolecules. 2009 ; 10: 3157-3175
    • (2009) Biomacromolecules , vol.10 , pp. 3157-3175
    • Manakker, F.1    Vermonden, T.2    Nostrum, C.F.3
  • 17
    • 68949214375 scopus 로고    scopus 로고
    • Lipid nanocapsules: A new platform for nanomedicine
    • Huynh NT, Passirani C, Saulnier P, et al. Lipid nanocapsules: a new platform for nanomedicine. Int J Pharm. 2009 ; 379: 201-209
    • (2009) Int J Pharm , vol.379 , pp. 201-209
    • Huynh, N.T.1    Passirani, C.2    Saulnier, P.3
  • 18
    • 60549091179 scopus 로고    scopus 로고
    • Multifunctional micellar nanomedicine for cancer therapy
    • Blanco E, Kessinger CW, Sumer BD, et al. Multifunctional micellar nanomedicine for cancer therapy. Exp Biol Med (Maywood). 2009 ; 234(2): 123-131
    • (2009) Exp Biol Med (Maywood) , vol.2342 , pp. 123-131
    • Blanco, E.1    Kessinger, C.W.2    Sumer, B.D.3
  • 19
    • 34249023676 scopus 로고    scopus 로고
    • Functionalized micellar systems for cancer targeted drug delivery
    • Sutton D, Nasongkla N, Blanco E, et al. Functionalized micellar systems for cancer targeted drug delivery. Pharm Res. 2007 ; 24(6): 1029-1046
    • (2007) Pharm Res , vol.246 , pp. 1029-1046
    • Sutton, D.1    Nasongkla, N.2    Blanco, E.3
  • 20
    • 1542298887 scopus 로고    scopus 로고
    • Poly(N-isopropylacrylamide) copolymers for constant temperature controlled drug delivery
    • Moës AJ, Amighi K, Eeckman F. Poly(N-isopropylacrylamide) copolymers for constant temperature controlled drug delivery. Int J Pharm. 2004 ; 273: 109-119
    • (2004) Int J Pharm , vol.273 , pp. 109-119
    • Moës, A.J.1    Amighi, K.2    Eeckman, F.3
  • 21
    • 34248588338 scopus 로고    scopus 로고
    • Difunctional pluronic copolymer micelles for paclitaxel delivery: Synergistic effect of folate-mediated targeting and pluronic-mediated overcoming multidrug resistance in tumor cell lines
    • Wang YZ, Li YJ, Han LM, et al. Difunctional pluronic copolymer micelles for paclitaxel delivery: synergistic effect of folate-mediated targeting and pluronic-mediated overcoming multidrug resistance in tumor cell lines. Int J Pharm. 2007 ; 337: 63-73
    • (2007) Int J Pharm , vol.337 , pp. 63-73
    • Wang, Y.Z.1    Li, Y.J.2    Han, L.M.3
  • 22
    • 79951576538 scopus 로고    scopus 로고
    • Multifunctional pluronic P123/F127 mixed polymeric micelles loaded with paclitaxel for the treatment of multidrug resistant tumors
    • Zhang W, Shi Y, Chen Y, et al. Multifunctional pluronic P123/F127 mixed polymeric micelles loaded with paclitaxel for the treatment of multidrug resistant tumors. Biomaterials. 2011 ; 32: 2894-2906
    • (2011) Biomaterials , vol.32 , pp. 2894-2906
    • Zhang, W.1    Shi, Y.2    Chen, Y.3
  • 23
    • 0018387446 scopus 로고
    • Promotion of microtubule assembly in vitro by taxol
    • Schiff PB, Horwitz SB. Promotion of microtubule assembly in vitro by taxol. Nature. 1979 ; 277: 665-667
    • (1979) Nature , vol.277 , pp. 665-667
    • Schiff, P.B.1    Horwitz, S.B.2
  • 24
    • 57349142938 scopus 로고    scopus 로고
    • Targeting the delivery of glycan-based paclitaxel prodrugs to cancer cells via glucose transporters
    • Lin YS, Tungpradit R, Sinchaikul S, et al. Targeting the delivery of glycan-based paclitaxel prodrugs to cancer cells via glucose transporters. J Med Chem. 2008 ; 51: 7428-7441
    • (2008) J Med Chem , vol.51 , pp. 7428-7441
    • Lin, Y.S.1    Tungpradit, R.2    Sinchaikul, S.3
  • 25
    • 0026567883 scopus 로고
    • Synthesis and evaluation of some water-soluble prodrugs and derivatives of taxol with antitumor activity
    • Mathew AE, Mejillano MR, Nath JP, et al. Synthesis and evaluation of some water-soluble prodrugs and derivatives of taxol with antitumor activity. J Med Chem. 1992 ; 35: 145-151
    • (1992) J Med Chem , vol.35 , pp. 145-151
    • Mathew, A.E.1    Mejillano, M.R.2    Nath, J.P.3
  • 26
    • 67349137876 scopus 로고    scopus 로고
    • Paclitaxel-loaded pluronic P123/F127 mixed polymeric micelles: Formulation, optimization and in vitro characterization
    • Zhang W, Hao J, Shi Y, et al. Paclitaxel-loaded pluronic P123/F127 mixed polymeric micelles: formulation, optimization and in vitro characterization. Int J Pharm. 2009 ; 376: 176-185
    • (2009) Int J Pharm , vol.376 , pp. 176-185
    • Zhang, W.1    Hao, J.2    Shi, Y.3
  • 27
    • 78649775109 scopus 로고    scopus 로고
    • Paclitaxel-loaded pluronic nanoparticles formed by a temperature-induced phase transition for cancer therapy
    • Oh KS, Song JY, Cho SH, et al. Paclitaxel-loaded pluronic nanoparticles formed by a temperature-induced phase transition for cancer therapy. J Control Release. 2010 ; 148: 344-350
    • (2010) J Control Release , vol.148 , pp. 344-350
    • Oh, K.S.1    Song, J.Y.2    Cho, S.H.3
  • 28
    • 0029980834 scopus 로고    scopus 로고
    • Development of amphiphilic diblock copolymers as micellar carriers of taxol
    • Zhang X, Jackson JK, Burt HM. Development of amphiphilic diblock copolymers as micellar carriers of taxol. Int J Pharm. 1996 ; 132: 195-206
    • (1996) Int J Pharm , vol.132 , pp. 195-206
    • Zhang, X.1    Jackson, J.K.2    Burt, H.M.3
  • 29
    • 13844292729 scopus 로고    scopus 로고
    • Dynamic monitoring of cytotoxicity on microelectronic sensors
    • Xing JZ, Zhu L, Jackson JA, et al. Dynamic monitoring of cytotoxicity on microelectronic sensors. Chem Res Toxicol. 2005 ; 18(2): 154-161
    • (2005) Chem Res Toxicol , vol.182 , pp. 154-161
    • Xing, J.Z.1    Zhu, L.2    Jackson, J.A.3
  • 30
    • 44749086918 scopus 로고    scopus 로고
    • Development and validation of HPLC method for the determination of tobramycin in urine samples post-inhalation using pre-column derivatisation with fluorescein isothiocyanate
    • Mashat M, Chrystyn H, Clark BJ, et al. Development and validation of HPLC method for the determination of tobramycin in urine samples post-inhalation using pre-column derivatisation with fluorescein isothiocyanate. J Chromatogr B. 2008 ; 869: 59-66
    • (2008) J Chromatogr B , vol.869 , pp. 59-66
    • Mashat, M.1    Chrystyn, H.2    Clark, B.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.