메뉴 건너뛰기




Volumn 10, Issue 3, 2013, Pages 325-340

Paclitaxel drug delivery systems

Author keywords

Cancer nanotechnology; Drug delivery systems; Drug formulation; Nanomedicine; Pharmaceutical nanotechnology; Taxanes

Indexed keywords

CYPHER DRUG; DENDRIMER; DOCETAXEL; LIPOSOME; PACLITAXEL; POLYMER; PRODRUG; RAPAMYCIN; SOLID LIPID NANOPARTICLE; TAXUS DRUG; UNCLASSIFIED DRUG;

EID: 84873887585     PISSN: 17425247     EISSN: 17447593     Source Type: Journal    
DOI: 10.1517/17425247.2013.752354     Document Type: Review
Times cited : (158)

References (100)
  • 2
    • 0015211527 scopus 로고
    • Plant anti-tumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
    • Wani MC, Taylor HL, Wall ME, et al. Plant anti-tumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J Am Chem Soc 1971;93:2325-7
    • (1971) J Am Chem Soc , vol.93 , pp. 2325-2327
    • Wani, M.C.1    Taylor, H.L.2    Wall, M.E.3
  • 3
    • 57349119942 scopus 로고    scopus 로고
    • Pharmaceutical aspects of drug eluting stents
    • Deconinck E, Sohier J, De Scheerder I. Pharmaceutical aspects of drug eluting stents. J Pharm Sci 2008;97:5047-60
    • (2008) J Pharm Sci , vol.97 , pp. 5047-5060
    • Deconinck, E.1    Sohier, J.2    De Scheerder, I.3
  • 4
    • 78650254061 scopus 로고    scopus 로고
    • Production of the anticancer drug taxol in Taxus baccata suspension cultures
    • Sonia M, Cusidó RM, Mirjalili MH, et al. Production of the anticancer drug taxol in Taxus baccata suspension cultures. Process Biochem 2011;46:23-34
    • (2011) Process Biochem , vol.46 , pp. 23-34
    • Sonia, M.1    Cusidó, R.M.2    Mirjalili, M.H.3
  • 5
    • 0000052734 scopus 로고
    • Taxol and taxotere: Discovery, chemistry and structure activity relationship
    • Guenard D, Gueritte-Voegelein F, Poiter P. Taxol and taxotere: discovery, chemistry and structure activity relationship. Acc Chem Res 1993;26:160-7
    • (1993) Acc Chem Res , vol.26 , pp. 160-167
    • Guenard, D.1    Gueritte-Voegelein, F.2    Poiter, P.3
  • 6
    • 67651115890 scopus 로고    scopus 로고
    • Recent advances in the study of the bioactive conformation of taxol
    • Sun L, Simmerling C, Ojima I. Recent advances in the study of the bioactive conformation of taxol. Chem Med Chem 2009;4:719-31
    • (2009) Chem Med Chem , vol.4 , pp. 719-731
    • Sun, L.1    Simmerling, C.2    Ojima, I.3
  • 7
    • 0034212385 scopus 로고    scopus 로고
    • Paclitaxel-induced cell death: Where the cell cycle and apoptosis come together
    • Wang TH, Wang HS, Soong YK. Paclitaxel-induced cell death: where the cell cycle and apoptosis come together. Cancer 2000;88:2619-28
    • (2000) Cancer , vol.88 , pp. 2619-2628
    • Wang, T.H.1    Wang, H.S.2    Soong, Y.K.3
  • 8
    • 0034041275 scopus 로고    scopus 로고
    • Recent advances in the chemistry of taxol
    • DOI 10.1021/np000064n
    • Kingston DG. Recent advances in the chemistry of Taxol. J Nat Prod 2000;63:726-34 (Pubitemid 30395547)
    • (2000) Journal of Natural Products , vol.63 , Issue.5 , pp. 726-734
    • Kingston, D.G.I.1
  • 10
    • 0035003021 scopus 로고    scopus 로고
    • Role of formulation vehicles in taxane pharmacology
    • DOI 10.1023/A:1010618632738
    • Van Zuylen L, Verweij J, Sparreboom A. Role of formulation vehicles in taxane pharmacology. Invest New Drugs 2001;19:125-41 (Pubitemid 32423718)
    • (2001) Investigational New Drugs , vol.19 , Issue.2 , pp. 125-141
    • Van Zuylen, L.1    Verweij, J.2    Sparreboom, A.3
  • 11
    • 25144476858 scopus 로고    scopus 로고
    • Paclitaxel chemotherapy: From empiricism to a mechanism-based formulation strategy
    • Scripture CD, Figg WD, Sparreboom A. Paclitaxel chemotherapy: from empiricism to a mechanism-based formulation strategy. Ther Clin Risk Manag 2005;1:107-14
    • (2005) Ther Clin Risk Manag , vol.1 , pp. 107-114
    • Scripture, C.D.1    Figg, W.D.2    Sparreboom, A.3
  • 12
    • 82455175226 scopus 로고    scopus 로고
    • A phase 2 study of weekly albumin-bound paclitaxel (Abraxane) given as a two-hour infusion
    • Paik PK, James LP, Riely GJ, et al. A phase 2 study of weekly albumin-bound paclitaxel (Abraxane) given as a two-hour infusion. Cancer Chemother Pharmacol 2011;68:1331-7
    • (2011) Cancer Chemother Pharmacol , vol.68 , pp. 1331-1337
    • Paik, P.K.1    James, L.P.2    Riely, G.J.3
  • 13
    • 7444253306 scopus 로고    scopus 로고
    • Prodrug research: Futile or fertile?
    • DOI 10.1016/j.bcp.2004.07.005, PII S0006295204004745
    • Testa B. Prodrug research: futile or fertile? Biochem Pharmacol 2004;68:2097-106 (Pubitemid 39446137)
    • (2004) Biochemical Pharmacology , vol.68 , Issue.11 , pp. 2097-2106
    • Testa, B.1
  • 15
    • 33845508580 scopus 로고    scopus 로고
    • Paclitaxel prodrugs: Toward smarter delivery of anticancer agents
    • DOI 10.1021/jm0602155
    • Skwarczynski M, Hayashi Y, Kiso Y. Paclitaxel prodrugs: toward smarter delivery of anticancer agents. J Med Chem 2006;49:7253-69 (Pubitemid 44913386)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.25 , pp. 7253-7269
    • Skwarczynski, M.1    Hayashi, Y.2    Kiso, Y.3
  • 16
    • 84856544910 scopus 로고    scopus 로고
    • A thermally responsive biopolymer conjugated to an acid-sensitive derivative of paclitaxel stabilizes microtubules, arrests cell cycle, and induces apoptosis
    • Moktan S, Ryppa C, Kratz F, et al. A thermally responsive biopolymer conjugated to an acid-sensitive derivative of paclitaxel stabilizes microtubules, arrests cell cycle, and induces apoptosis. Invest New Drugs 2012;30:236-48
    • (2012) Invest New Drugs , vol.30 , pp. 236-248
    • Moktan, S.1    Ryppa, C.2    Kratz, F.3
  • 17
    • 1442359716 scopus 로고    scopus 로고
    • Enhanced paclitaxel bioavailability after oral administration of pegylated paclitaxel prodrug for oral delivery in rats
    • Choi JS, Jo BW, Kim YC. Enhanced paclitaxel bioavailability after oral administration of pegylated paclitaxel prodrug for oral delivery in rats. Eur J Pharm Biopharm 2004;57:313-18
    • (2004) Eur J Pharm Biopharm , vol.57 , pp. 313-318
    • Choi, J.S.1    Jo, B.W.2    Kim, Y.C.3
  • 18
    • 33947216212 scopus 로고    scopus 로고
    • Microbial biosynthesis of polyglutamic acid biopolymer and applications in the biopharmaceutical, biomedical and food industries
    • DOI 10.1080/07388550601166458, PII 773236840
    • Buescher JM, Margaritis A. Microbial biosynthesis of polyglutamic acid biopolymer and applications in the biopharmaceutical, biomedical and food industries. Crit Rev Biotechnol 2007;27:1-19 (Pubitemid 46425931)
    • (2007) Critical Reviews in Biotechnology , vol.27 , Issue.1 , pp. 1-19
    • Buescher, J.M.1    Margaritis, A.2
  • 21
    • 50349101826 scopus 로고    scopus 로고
    • Randomized phase III trial comparing single-agent paclitaxel poliglumex (CT- 2103, PPX) with single-agent gemcitabine or vinorelbine for the treatment of PS 2 patients with chemotherapy-naive advanced non-small cell lung cancer
    • O'Brien ME, Socinski MA, Popovich AY, et al. Randomized phase III trial comparing single-agent paclitaxel poliglumex (CT- 2103, PPX) with single-agent gemcitabine or vinorelbine for the treatment of PS 2 patients with chemotherapy-naive advanced non-small cell lung cancer. J Thorac Oncol 2008;3:728-34
    • (2008) J Thorac Oncol , vol.3 , pp. 728-734
    • O'Brien, M.E.1    Socinski, M.A.2    Popovich, A.Y.3
  • 22
    • 66449130503 scopus 로고    scopus 로고
    • Enhanced cytotoxicity of a polymer-drug conjugate with triple payload of paclitaxel
    • Erez R, Segal E,Miller K, et al. Enhanced cytotoxicity of a polymer-drug conjugate with triple payload of paclitaxel. Bioorg Med Chem 2009;17:4327-35
    • (2009) Bioorg Med Chem , vol.17 , pp. 4327-4335
    • Erez, R.1    Segal, E.2    Miller, K.3
  • 23
    • 72449141425 scopus 로고    scopus 로고
    • Heparin-paclitaxel conjugates as drug delivery system: Synthesis, self-assembly property, drug release, and antitumor activity
    • Wang Y, Xin D, Liu K, et al. Heparin-paclitaxel conjugates as drug delivery system: synthesis, self-assembly property, drug release, and antitumor activity. Bioconjug Chem 2009;20:2214-21
    • (2009) Bioconjug Chem , vol.20 , pp. 2214-2221
    • Wang, Y.1    Xin, D.2    Liu, K.3
  • 24
    • 79958788003 scopus 로고    scopus 로고
    • Polymeric micelles with water-insoluble drug as hydrophobic moiety for drug delivery
    • Li GL, Liu JY, Pang Y, et al. Polymeric micelles with water-insoluble drug as hydrophobic moiety for drug delivery. Biomacromolecules 2011;12(6):2016-26
    • (2011) Biomacromolecules , vol.12 , Issue.6 , pp. 2016-2026
    • Li, G.L.1    Liu, J.Y.2    Pang, Y.3
  • 25
    • 84863229418 scopus 로고    scopus 로고
    • Antitumor activity and molecular dynamics simulations of paclitaxel-laden triazine dendrimers
    • Lim J, Lo ST, Hill S, et al. Antitumor activity and molecular dynamics simulations of paclitaxel-laden triazine dendrimers. Mol Pharm 2012;9:404-12
    • (2012) Mol Pharm , vol.9 , pp. 404-412
    • Lim, J.1    Lo, S.T.2    Hill, S.3
  • 26
    • 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;51:7428-41
    • (2008) J Med Chem , vol.51 , pp. 7428-7441
    • Lin, Y.S.1    Tungpradit, R.2    Sinchaikul, S.3
  • 27
    • 78649634752 scopus 로고    scopus 로고
    • Development of a novel prodrug of paclitaxel that is cleaved by prostate-specific antigen: An in vitro and in vivo evaluation study
    • Elsadek B, Graeser R, Esser N, et al. Development of a novel prodrug of paclitaxel that is cleaved by prostate-specific antigen: An in vitro and in vivo evaluation study. Eur J Cancer 2010;46:3434-4
    • (2010) Eur J Cancer , vol.46 , pp. 3434-3434
    • Elsadek, B.1    Graeser, R.2    Esser, N.3
  • 28
    • 77249172711 scopus 로고    scopus 로고
    • Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy
    • Quiles S, Raisch KP, Sanford L, et al. Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy. J Med Chem 2010;53:586-94
    • (2010) J Med Chem , vol.53 , pp. 586-594
    • Quiles, S.1    Raisch, K.P.2    Sanford, L.3
  • 29
    • 79952745545 scopus 로고    scopus 로고
    • Integrin-assisted drug delivery of nano-scaled polymer therapeutics bearing paclitaxel
    • Eldar-Boock A, Miller K, Sanchis J, et al. Integrin-assisted drug delivery of nano-scaled polymer therapeutics bearing paclitaxel. Biomaterials 2011;32:3862-74
    • (2011) Biomaterials , vol.32 , pp. 3862-3874
    • Eldar-Boock, A.1    Miller, K.2    Sanchis, J.3
  • 30
    • 82855172119 scopus 로고    scopus 로고
    • A paclitaxel-conjugated adenovirus vector for targeted drug delivery for tumor therapy
    • Shan L, Cui S, Du C, et al. A paclitaxel-conjugated adenovirus vector for targeted drug delivery for tumor therapy. Biomaterials 2012;33:146-62
    • (2012) Biomaterials , vol.33 , pp. 146-162
    • Shan, L.1    Cui, S.2    Du, C.3
  • 31
    • 68949136812 scopus 로고    scopus 로고
    • Phase 2 open-label study of weekly docosahexaenoic acid-paclitaxel in cutaneous and mucosal metastatic melanoma patients
    • Homsi J, Bedikian AY, Kim KB, et al. Phase 2 open-label study of weekly docosahexaenoic acid-paclitaxel in cutaneous and mucosal metastatic melanoma patients. Melanoma Res 2009;19:238-42
    • (2009) Melanoma Res , vol.19 , pp. 238-242
    • Homsi, J.1    Bedikian, A.Y.2    Kim, K.B.3
  • 32
    • 79953324540 scopus 로고    scopus 로고
    • Phase 3 study of docosahexaenoic acid-paclitaxel versus dacarbazine in patients with metastatic malignant melanoma
    • Bedikian AY, DeConti RC, Conry R, et al. Phase 3 study of docosahexaenoic acid-paclitaxel versus dacarbazine in patients with metastatic malignant melanoma. Ann Oncol 2011;22:787-93
    • (2011) Ann Oncol , vol.22 , pp. 787-793
    • Bedikian, A.Y.1    Deconti, R.C.2    Conry, R.3
  • 33
    • 77953081486 scopus 로고    scopus 로고
    • The therapeutic efficacy of conjugated linoleic acid - paclitaxel on glioma in the rat
    • Ke XY, Zhao BJ, Zhao X, et al. The therapeutic efficacy of conjugated linoleic acid - paclitaxel on glioma in the rat. Biomaterials 2010;31:5855-64
    • (2010) Biomaterials , vol.31 , pp. 5855-5864
    • Ke, X.Y.1    Zhao, B.J.2    Zhao, X.3
  • 34
    • 62549144354 scopus 로고    scopus 로고
    • Development of protein-binding bifunctional linkers for a new generation of dual-acting prodrugs
    • Abu Ajaj K, Biniossek ML, Kratz F. Development of protein-binding bifunctional linkers for a new generation of dual-acting prodrugs. Bioconjug Chem 2009;20:390-6
    • (2009) Bioconjug Chem , vol.20 , pp. 390-396
    • Abu Ajaj, K.1    Biniossek, M.L.2    Kratz, F.3
  • 35
    • 84863565467 scopus 로고    scopus 로고
    • A prodrug strategy to deliver cisplatin (IV) and paclitaxel in nanomicelles to improve efficacy and tolerance
    • Xiao H, Song H, Yang Q, et al. A prodrug strategy to deliver cisplatin (IV) and paclitaxel in nanomicelles to improve efficacy and tolerance. Biomaterials 2012;33:6507-19
    • (2012) Biomaterials , vol.33 , pp. 6507-6519
    • Xiao, H.1    Song, H.2    Yang, Q.3
  • 37
    • 80053609978 scopus 로고    scopus 로고
    • Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel-polymer micelles to overcome multi-drug resistance
    • Wang F, Zhang D, Zhang Q, et al. Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel-polymer micelles to overcome multi-drug resistance. Biomaterials 2011;32:9444-56
    • (2011) Biomaterials , vol.32 , pp. 9444-9456
    • Wang, F.1    Zhang, D.2    Zhang, Q.3
  • 39
    • 84860340286 scopus 로고    scopus 로고
    • Supramolecular micellar nanoaggregates based on a novel chitosan/vitamin e succinate copolymer for paclitaxel selective delivery
    • Lian H, Sun J, Yu YP, et al. Supramolecular micellar nanoaggregates based on a novel chitosan/vitamin E succinate copolymer for paclitaxel selective delivery. Int J Nanomed 2011;6:3323-34
    • (2011) Int J Nanomed , vol.6 , pp. 3323-3334
    • Lian, H.1    Sun, J.2    Yu, Y.P.3
  • 41
    • 84866735036 scopus 로고    scopus 로고
    • Phase II study of NK105, a paclitaxel-incorporating micellar nanoparticle, for previously treated advanced or recurrent gastric cancer
    • Kato K, Chin K, Yoshikawa T, et al. Phase II study of NK105, a paclitaxel-incorporating micellar nanoparticle, for previously treated advanced or recurrent gastric cancer. Invest New Drugs 2012;30:1621-7
    • (2012) Invest New Drugs , vol.30 , pp. 1621-1627
    • Kato, K.1    Chin, K.2    Yoshikawa, T.3
  • 42
    • 33748289523 scopus 로고    scopus 로고
    • NK105, a paclitaxel-incorporating micellar nanoparticle, is a more potent radiosensitising agent compared to free paclitaxel
    • DOI 10.1038/sj.bjc.6603311, PII 6603311
    • Negishi T, Koizumi F, Uchino H, et al. NK105, a paclitaxel-incorporating micellar nanoparticle, is a more potent radiosensitising agent compared to free paclitaxel. Br J Cancer 2006;95:601-6 (Pubitemid 44325900)
    • (2006) British Journal of Cancer , vol.95 , Issue.5 , pp. 601-606
    • Negishi, T.1    Koizumi, F.2    Uchino, H.3    Kuroda, J.4    Kawaguchi, T.5    Naito, S.6    Matsumura, Y.7
  • 44
    • 78149342494 scopus 로고    scopus 로고
    • Enhanced oral absorption of paclitaxel in N-deoxycholic acid-N, O-hydroxyethyl chitosan micellar system
    • Li H, Huo M, Zhou J, et al. Enhanced oral absorption of paclitaxel in N-deoxycholic acid-N, O-hydroxyethyl chitosan micellar system. J Pharm Sci 2010;99:4543-53
    • (2010) J Pharm Sci , vol.99 , pp. 4543-4553
    • Li, H.1    Huo, M.2    Zhou, J.3
  • 45
    • 0035858296 scopus 로고    scopus 로고
    • In vivo evaluation of polymeric micellar paclitaxel formulation: Toxicity and efficacy
    • DOI 10.1016/S0168-3659(01)00275-9, PII S0168365901002759
    • Kim SC, Kim DW, Shim YH, et al. In vivo evaluation of polymeric micellar paclitaxel formulation: toxicity and efficacy. J Control Release 2001;72:191-202 (Pubitemid 32522357)
    • (2001) Journal of Controlled Release , vol.72 , Issue.1-3 , pp. 191-202
    • Kim, S.C.1    Kim, D.W.2    Shim, Y.H.3    Bang, J.S.4    Oh, H.S.5    Kim, S.W.6    Seo, M.H.7
  • 46
    • 2542559832 scopus 로고    scopus 로고
    • Phase i and pharmacokinetic study of Genexol-PM, a cremophor-free, polymeric micelle-formulated paclitaxel, in patients with advanced malignancies
    • Kim TY, Kim DW, Chung JY, et al. Phase I and pharmacokinetic study of Genexol-PM, a cremophor-free, polymeric micelle-formulated paclitaxel, in patients with advanced malignancies. Clin Cancer Res 2004;10:3708-16
    • (2004) Clin Cancer Res , vol.10 , pp. 3708-3716
    • Kim, T.Y.1    Kim, D.W.2    Chung, J.Y.3
  • 47
    • 80054110603 scopus 로고    scopus 로고
    • Development of docetaxel-loaded intravenous formulation, Nanoxel-PM using polymer-based delivery system
    • Lee SW, Yun MH, Jeong SW, et al. Development of docetaxel-loaded intravenous formulation, Nanoxel-PM using polymer-based delivery system. J Control Release 2011;155:262-71
    • (2011) J Control Release , vol.155 , pp. 262-271
    • Lee, S.W.1    Yun, M.H.2    Jeong, S.W.3
  • 48
    • 54049090061 scopus 로고    scopus 로고
    • Antibody-modified liposomes for cancer chemotherapy
    • Torchilin V. Antibody-modified liposomes for cancer chemotherapy. Expert Opin Drug Del 2008;5:1003-25
    • (2008) Expert Opin Drug Del , vol.5 , pp. 1003-1025
    • Torchilin, V.1
  • 50
    • 66449130503 scopus 로고    scopus 로고
    • Enhanced cytotoxicity of a polymer-drug conjugate with triple payload of paclitaxel
    • Erez R, Segal E, Miller K, et al. Enhanced cytotoxicity of a polymer-drug conjugate with triple payload of paclitaxel. Bioorg Med Chem 2009;17:4327-35
    • (2009) Bioorg Med Chem , vol.17 , pp. 4327-4335
    • Erez, R.1    Segal, E.2    Miller, K.3
  • 51
    • 70349374079 scopus 로고    scopus 로고
    • A study on antitumor effect of liposome encapsulated paclitaxel in vivo and in vitro
    • Yang AZ, Li J, Xu HJ, et al. A study on antitumor effect of liposome encapsulated paclitaxel in vivo and in vitro. Bull Chin Cancer 2006;15:862-4
    • (2006) Bull Chin Cancer , vol.15 , pp. 862-864
    • Yang, A.Z.1    Li, J.2    Xu, H.J.3
  • 52
    • 84856647388 scopus 로고    scopus 로고
    • Membrane biophysical parameters influencing anthracycline action
    • Priebe W Editor. Anthracycline Antibiotics. New York: American Chemical Society Publication
    • Mehta RR, Burke TG. Membrane biophysical parameters influencing anthracycline action. Anthracycline antibiotics. In: Priebe W, editor. Anthracycline Antibiotics. New York: American Chemical Society Publication; 2004:222-40
    • (2004) Anthracycline Antibiotics , pp. 222-240
    • Mehta, R.R.1    Burke, T.G.2
  • 53
    • 11144283530 scopus 로고    scopus 로고
    • Paclitaxel quantification in mouse plasma and tissues containing liposome-entrapped paclitaxel by liquid chromatography-tandem mass spectrometry: Application to a pharmacokinetics study
    • DOI 10.1016/j.ab.2004.09.046, PII S0003269704008012
    • GuoW, Johnson JL, Khan S, et al. Paclitaxel quantification in mouse plasma and tissues containing liposome-entrapped paclitaxel by liquid chromatographytandem mass spectrometry: application to a pharmacokinetics study. Anal Biochem 2005;336:213-20 (Pubitemid 40038019)
    • (2005) Analytical Biochemistry , vol.336 , Issue.2 , pp. 213-220
    • Guo, W.1    Johnson, J.L.2    Khan, S.3    Ahmad, A.4    Ahmad, I.5
  • 54
    • 53249131199 scopus 로고    scopus 로고
    • Pharmacokinetic/pharmacodynamic modeling and simulation of neutropenia during phase i development of liposome-entrapped paclitaxel
    • Fetterly GJ, Grasela TH, Sherman JW, et al. Pharmacokinetic/ pharmacodynamic modeling and simulation of neutropenia during phase I development of liposome-entrapped paclitaxel. Clin Cancer Res 2008;14:5856-63
    • (2008) Clin Cancer Res , vol.14 , pp. 5856-5863
    • Fetterly, G.J.1    Grasela, T.H.2    Sherman, J.W.3
  • 56
    • 84856638259 scopus 로고    scopus 로고
    • Clinical development of liposome-based drugs: Formulation, characterization, and therapeutic efficacy
    • Chang HI, Yeh MK. Clinical development of liposome-based drugs: formulation, characterization, and therapeutic efficacy. Int J Nanomedicine 2012;7:49-60
    • (2012) Int J Nanomedicine , vol.7 , pp. 49-60
    • Chang, H.I.1    Yeh, M.K.2
  • 57
    • 84864013044 scopus 로고    scopus 로고
    • Polyelectrolyte stabilized multilayered liposomes for oral delivery of paclitaxel
    • Jain S, Kumar D, Swarnakar NK, et al. Polyelectrolyte stabilized multilayered liposomes for oral delivery of paclitaxel. Biomaterials 2012;33:6758-68
    • (2012) Biomaterials , vol.33 , pp. 6758-6768
    • Jain, S.1    Kumar, D.2    Swarnakar, N.K.3
  • 58
    • 84860640294 scopus 로고    scopus 로고
    • Absorption, disposition and pharmacokinetics of solid lipid nanoparticles
    • Qi J, Lu Y, Wu W. Absorption, disposition and pharmacokinetics of solid lipid nanoparticles. Curr Drug Metab 2012;13:418-28
    • (2012) Curr Drug Metab , vol.13 , pp. 418-428
    • Qi, J.1    Lu, Y.2    Wu, W.3
  • 59
    • 37249078585 scopus 로고    scopus 로고
    • Cellular uptake of solid lipid nanoparticles and cytotoxicity of encapsulated paclitaxel in A549 cancer cells
    • DOI 10.1016/j.ijpharm.2007.07.012, PII S0378517307005960
    • Yuan H, Miao J, Du YZ, et al. Cellular uptake of solid lipid nanoparticles and cytotoxicity of encapsulated paclitaxel in A549 cancer cells. Int J Pharm 2008;348:137-45 (Pubitemid 350266242)
    • (2008) International Journal of Pharmaceutics , vol.348 , Issue.1-2 , pp. 137-145
    • Yuan, H.1    Miao, J.2    Du, Y.-Z.3    You, J.4    Hu, F.-Q.5    Zeng, S.6
  • 60
    • 33846677328 scopus 로고    scopus 로고
    • Preparation, characterization and in vitro cytotoxicity of paclitaxel-loaded sterically stabilized solid lipid nanoparticles
    • Lee MK, Lim SJ, Kim CK. Preparation, characterization and in vitro cytotoxicity of paclitaxel-loaded sterically stabilized solid lipid nanoparticles. Biomaterials 2007;28:2137-46
    • (2007) Biomaterials , vol.28 , pp. 2137-2146
    • Lee, M.K.1    Lim, S.J.2    Kim, C.K.3
  • 61
    • 0034760365 scopus 로고    scopus 로고
    • In vitro and in vivo study of two types of long-circulating solid lipid nanoparticles containing paclitaxel
    • Chen DB, Yang TZ, Lu WL. In vitro and in vivo study of two types of long-circulating solid lipid nanoparticles containing paclitaxel. Chem Pharm Bull 2001;49:1444-7
    • (2001) Chem Pharm Bull , vol.49 , pp. 1444-1447
    • Chen, D.B.1    Yang, T.Z.2    Lu, W.L.3
  • 62
    • 65949120534 scopus 로고    scopus 로고
    • Doxorubicin and paclitaxel-loaded lipid-based nanoparticles overcome multidrug resistance by inhibiting P-glycoprotein and depleting ATP
    • Dong XW, Mattingly CA, Tseng MT, et al. Doxorubicin and paclitaxel-loaded lipid-based nanoparticles overcome multidrug resistance by inhibiting P-glycoprotein and depleting ATP. Cancer Res 2009;69:3918-26
    • (2009) Cancer Res , vol.69 , pp. 3918-3926
    • Dong, X.W.1    Mattingly, C.A.2    Tseng, M.T.3
  • 63
    • 4544240398 scopus 로고    scopus 로고
    • Paclitaxel nanoparticles for the potential treatment of brain tumors
    • DOI 10.1016/j.jconrel.2004.07.006, PII S0168365904003141
    • Koziara JM, Lockman PR, Allen DD, Mumper RJ. Paclitaxel nanoparticles for the potential treatment of brain tumors. J Control Release 2004;99:259-69 (Pubitemid 39222111)
    • (2004) Journal of Controlled Release , vol.99 , Issue.2 , pp. 259-269
    • Koziara, J.M.1    Lockman, P.R.2    Allen, D.D.3    Mumper, R.J.4
  • 64
    • 84866484085 scopus 로고    scopus 로고
    • Solid lipid nanoparticles of paclitaxel strengthened by hydroxypropyl-beta-cyclodextrin as an oral delivery system
    • Baek JS, So JW, Shin SC, et al. Solid lipid nanoparticles of paclitaxel strengthened by hydroxypropyl-beta-cyclodextrin as an oral delivery system. Int J Mol Med 2012;30:953-9
    • (2012) Int J Mol Med , vol.30 , pp. 953-959
    • Baek, J.S.1    So, J.W.2    Shin, S.C.3
  • 65
    • 28844438726 scopus 로고    scopus 로고
    • In vitro and in vivo studies on vitamin E TPGS-emulsified poly(D,L-lactic-co-glycolic acid) nanoparticles for paclitaxel formulation
    • DOI 10.1016/j.biomaterials.2005.11.008, PII S0142961205010355
    • Win KY, Feng SS. In vitro and in vivo studies on vitamin E TPGS-emulsified poly(D,L-lactic-co-glycolic acid) nanoparticles for paclitaxel formulation. Biomaterials 2006;27:2285-91 (Pubitemid 41774539)
    • (2006) Biomaterials , vol.27 , Issue.10 , pp. 2285-2291
    • Win, K.Y.1    Feng, S.-S.2
  • 66
    • 35349017895 scopus 로고    scopus 로고
    • Chemotherapeutic engineering: Vitamin E TPGS-emulsified nanoparticles of biodegradable polymers realized sustainable paclitaxel chemotherapy for 168 h in vivo
    • DOI 10.1016/j.ces.2007.08.006, PII S000925090700629X
    • Feng SS, Zhao L, Zhang Z. Chemotherapeutic engineering: vitamin E TPGS-emulsified nanoparticles of biodegradable polymers realized sustainable paclitaxel chemotherapy for 168 h in vivo. Chem Eng Sci 2007;62:6641-8 (Pubitemid 47610671)
    • (2007) Chemical Engineering Science , vol.62 , Issue.23 , pp. 6641-6648
    • Feng, S.-S.1    Zhao, L.2    Zhang, Z.3    Bhakta, G.4    Yin Win, K.5    Dong, Y.6    Chien, S.7
  • 67
    • 46749107462 scopus 로고    scopus 로고
    • In vitro and in vivo investigation on PLA-TPGS nanoparticles for controlled and sustained small molecule chemotherapy
    • Zhang ZP, Lee SH, Gan CW, et al. In vitro and in vivo investigation on PLA-TPGS nanoparticles for controlled and sustained small molecule chemotherapy. Pharm Res 2008;25:1925-35
    • (2008) Pharm Res , vol.25 , pp. 1925-1935
    • Zhang, Z.P.1    Lee, S.H.2    Gan, C.W.3
  • 68
    • 77955627105 scopus 로고    scopus 로고
    • Enhancement of Chemotherapeutical Efficacy of Docetaxel by Using a Biodegradable Nanoparticle Formulation
    • Gan CW, Chien S, Feng SS. Enhancement of Chemotherapeutical Efficacy of Docetaxel by Using a Biodegradable Nanoparticle Formulation. Curr Pharm Des 2011;16:2308-20
    • (2011) Curr Pharm des , vol.16 , pp. 2308-2320
    • Gan, C.W.1    Chien, S.2    Feng, S.S.3
  • 69
    • 84859839124 scopus 로고    scopus 로고
    • Vitamin e TPGS as a molecular biomaterial for drug delivery
    • Zhang ZP, Tan SW, Feng SS. Vitamin E TPGS as a molecular biomaterial for drug delivery. Biomaterials 2012;33:4889-906
    • (2012) Biomaterials , vol.33 , pp. 4889-4906
    • Zhang, Z.P.1    Tan, S.W.2    Feng, S.S.3
  • 70
    • 24644459310 scopus 로고    scopus 로고
    • Nanoparticles of poly(lactide)/vitamin e TPGS copolymer for cancer chemotherapy: Synthesis, formulation, characterization and in vitro drug release
    • Zhang ZP, Feng SS. Nanoparticles of poly(lactide)/vitamin E TPGS copolymer for cancer chemotherapy: synthesis, formulation, characterization and in vitro drug release. Biomaterials 2006;27:262-70
    • (2006) Biomaterials , vol.27 , pp. 262-270
    • Zhang, Z.P.1    Feng, S.S.2
  • 71
    • 33646032083 scopus 로고    scopus 로고
    • The drug encapsulation efficiency, in vitro drug release, cellular uptake and cytotoxicity of paclitaxel-loaded poly(lactide)-tocopheryl polyethylene glycol succinate nanoparticles
    • Zhang ZP, Feng SS. The drug encapsulation efficiency, in vitro drug release, cellular uptake and cytotoxicity of paclitaxel-loaded poly(lactide)-tocopheryl polyethylene glycol succinate nanoparticles. Biomaterials 2006;27:4025-33
    • (2006) Biomaterials , vol.27 , pp. 4025-4033
    • Zhang, Z.P.1    Feng, S.S.2
  • 72
    • 33749663431 scopus 로고    scopus 로고
    • Self-assembled nanoparticles of poly(lactide) - Vitamin e TPGS copolymers for oral chemotherapy
    • Zhang ZP, Feng SS. Self-assembled nanoparticles of poly(lactide) - Vitamin E TPGS copolymers for oral chemotherapy. Int J Pharm 2006;324:191-8
    • (2006) Int J Pharm , vol.324 , pp. 191-198
    • Zhang, Z.P.1    Feng, S.S.2
  • 73
    • 79959967718 scopus 로고    scopus 로고
    • Copolymer technology for advanced nanomedicine
    • Zhang ZP, Yang XL, Feng SS. Copolymer technology for advanced nanomedicine. Nanomedicine 2011;6:583-7
    • (2011) Nanomedicine , vol.6 , pp. 583-587
    • Zhang, Z.P.1    Yang, X.L.2    Feng, S.S.3
  • 74
    • 77955108815 scopus 로고    scopus 로고
    • Enhanced oral bioavailability of paclitaxel formulated in Vitamin E-TPGS emulsified nanoparticles of biodegradable polymers: In vitro and in vivo studies
    • Zhao LY, Feng SS. Enhanced oral bioavailability of paclitaxel formulated in Vitamin E-TPGS emulsified nanoparticles of biodegradable polymers: in vitro and in vivo studies. J Pharm Sci 2010;99:3552-60
    • (2010) J Pharm Sci , vol.99 , pp. 3552-3560
    • Zhao, L.Y.1    Feng, S.S.2
  • 75
    • 67349198099 scopus 로고    scopus 로고
    • Poly (lactide) - vitamin e derivative/ montmorillonite nanoparticle formulations for the oral delivery of Docetaxel
    • Feng SS, Mei L, Anitha P, et al. Poly (lactide) - vitamin E derivative/ montmorillonite nanoparticle formulations for the oral delivery of Docetaxel. Biomaterials 2009;30:3297-306
    • (2009) Biomaterials , vol.30 , pp. 3297-3306
    • Feng, S.S.1    Mei, L.2    Anitha, P.3
  • 76
    • 80053622909 scopus 로고    scopus 로고
    • Nanoformulation of d - A-tocopheryl polyethylene glycol 1000 succinate-b-poly ("-caprolactone-ran-glycolide) diblock copolymer for breast cancer therapy
    • Huang L, Chen H, Zheng Y, et al. Nanoformulation of d-a-tocopheryl polyethylene glycol 1000 succinate-b-poly ("-caprolactone-ran-glycolide) diblock copolymer for breast cancer therapy. Integr Biol 2011;3:951-1054
    • (2011) Integr Biol , vol.3 , pp. 951-1054
    • Huang, L.1    Chen, H.2    Zheng, Y.3
  • 77
    • 77956626333 scopus 로고    scopus 로고
    • A novel paclitaxel-loaded poly ("-caprolactone)/ poloxamer 188 blend nanoparticle overcoming multidrug resistance for cancer treatment
    • Zhang Y, Tang L, Sun L, et al. A novel paclitaxel-loaded poly ("-caprolactone)/ poloxamer 188 blend nanoparticle overcoming multidrug resistance for cancer treatment. Acta Biomater 2010;6:2045-52
    • (2010) Acta Biomater , vol.6 , pp. 2045-2052
    • Zhang, Y.1    Tang, L.2    Sun, L.3
  • 78
    • 34247639105 scopus 로고    scopus 로고
    • Modified paclitaxel-loaded nanoparticles for inhibition of hyperplasia in a rabbit arterial balloon injury model
    • DOI 10.1007/s11095-006-9214-z
    • Mei L, Sun H, Jin X, et al. Modified paclitaxel-loaded nanoparticles for inhibition of hyperplasia in a rabbit arterial balloon injury model. Pharm Res 2007;24:955-62 (Pubitemid 46675396)
    • (2007) Pharmaceutical Research , vol.24 , Issue.5 , pp. 955-962
    • Mei, L.1    Sun, H.2    Jin, X.3    Zhu, D.4    Sun, R.5    Zhang, M.6    Song, C.7
  • 79
    • 41949133558 scopus 로고    scopus 로고
    • Targeted delivery of paclitaxel using folate-decorated poly (lactide) vitamin e TPGS nanoparticles
    • Pan J, Feng SS. Targeted delivery of paclitaxel using folate-decorated poly (lactide) vitamin E TPGS nanoparticles. Biomaterials 2008;29:2663-72
    • (2008) Biomaterials , vol.29 , pp. 2663-2672
    • Pan, J.1    Feng, S.S.2
  • 80
    • 79959514159 scopus 로고    scopus 로고
    • Improved therapeutic effect of folate-decorated PLGA-PEG nanoparticles for endometrial carcinoma
    • Liang C, Yang Y, Ling Y, et al. Improved therapeutic effect of folate-decorated PLGA-PEG nanoparticles for endometrial carcinoma. Bioorg Med Chem 2011;19:4057-66
    • (2011) Bioorg Med Chem , vol.19 , pp. 4057-4066
    • Liang, C.1    Yang, Y.2    Ling, Y.3
  • 81
    • 70350571637 scopus 로고    scopus 로고
    • Dendrimers: Analytical characterization and applications v
    • Biricova V, Laznickova A. Dendrimers: analytical characterization and applications V. Bioorg Chem 2009;37:185-92
    • (2009) Bioorg Chem , vol.37 , pp. 185-192
    • Biricova, V.1    Laznickova, A.2
  • 83
    • 79956340892 scopus 로고    scopus 로고
    • Cancer targeting potential of some ligand-anchored poly(propylene imine dendrimers: A comparison
    • Kesharwani P, Tekade RK, Gajbhiye V, et al. Cancer targeting potential of some ligand-anchored poly(propylene imine dendrimers: a comparison. Nanomedicine 2011;7:295-304
    • (2011) Nanomedicine , vol.7 , pp. 295-304
    • Kesharwani, P.1    Tekade, R.K.2    Gajbhiye, V.3
  • 84
    • 49749126336 scopus 로고    scopus 로고
    • Receptor targeted polymers, dendrimers, liposomes: Which nanocarrier is the most efficient for tumor-specific treatment and imaging?
    • Saad M, Garbuzenko OB, Ber E, et al. Receptor targeted polymers, dendrimers, liposomes: which nanocarrier is the most efficient for tumor-specific treatment and imaging? J Control Release 2008;130:107-14
    • (2008) J Control Release , vol.130 , pp. 107-114
    • Saad, M.1    Garbuzenko, O.B.2    Ber, E.3
  • 85
    • 0242662544 scopus 로고    scopus 로고
    • Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel
    • DOI 10.1016/j.jconrel.2003.07.001
    • Ooya T, Lee J, Park K. Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel. J Control Release 2003;93:121-7 (Pubitemid 37421354)
    • (2003) Journal of Controlled Release , vol.93 , Issue.2 , pp. 121-127
    • Ooya, T.1    Lee, J.2    Park, K.3
  • 87
    • 33646388663 scopus 로고    scopus 로고
    • Restenosis related to percutaneous coronary intervention has been solved?
    • DOI 10.1080/07853890600643404, PII U2258708338173
    • Kivela A, Hartikainen J. Restenosis related to percutaneous coronary intervention has been solved? Ann Med 2006;38:173-87 (Pubitemid 43675583)
    • (2006) Annals of Medicine , vol.38 , Issue.3 , pp. 173-187
    • Kivela, A.1    Hartikainen, J.2
  • 89
    • 33847259689 scopus 로고    scopus 로고
    • Drug-eluting stent and coronary thrombosis: Biological mechanisms and clinical implications
    • DOI 10.1161/CIRCULATIONAHA.106.675934, PII 0000301720070227000016
    • Luscher TF, Steffel J, Eberli FR, et al. Drug-eluting stent and coronary thrombosis: biological mechanisms and clinical implications. Circulation 2007;115:1051-8 (Pubitemid 46328299)
    • (2007) Circulation , vol.115 , Issue.8 , pp. 1051-1058
    • Luscher, T.F.1    Steffel, J.2    Eberli, F.R.3    Joner, M.4    Nakazawa, G.5    Tanner, F.C.6    Virmani, R.7
  • 90
    • 84858155788 scopus 로고    scopus 로고
    • Drug eluting stents based on Poly (ethylene carbonate): Optimization of the stent coating process
    • Bege N, Steinmu?ller SO, Kalinowski M, et al. Drug eluting stents based on Poly (ethylene carbonate): optimization of the stent coating process. Eur J Pharm Biopharm 2012;80:562-70
    • (2012) Eur J Pharm Biopharm , vol.80 , pp. 562-570
    • Bege, N.1    Steinmuller, S.O.2    Kalinowski, M.3
  • 91
    • 79955622641 scopus 로고    scopus 로고
    • Editorial: Nanomedicine for oral chemotherapy
    • Feng SS, Zhao LY, Tang JT. Editorial: Nanomedicine for oral chemotherapy. Nanomedicine 2011;6:407-10
    • (2011) Nanomedicine , vol.6 , pp. 407-410
    • Feng, S.S.1    Zhao, L.Y.2    Tang, J.T.3
  • 92
    • 78650162093 scopus 로고    scopus 로고
    • New drug-eluting stents: An overview on biodegradable and polymer-free next-generation stent systems
    • Abizaid A, Costa Jr. New drug-eluting stents: an overview on biodegradable and polymer-free next-generation stent systems. Circ Cardiovasc Interv 2010;3:384-93
    • (2010) Circ Cardiovasc Interv , vol.3 , pp. 384-393
    • Abizaid, A.1    Costa, J.R.2
  • 93
    • 0037122675 scopus 로고    scopus 로고
    • Hydrogels for biomedical applications
    • DOI 10.1016/S0169-409X(01)00239-3, PII S0169409X01002393
    • Hoffman AS. Hydrogels for biomedical applications. Adv Drug Deliv Rev 2002;54:3-12 (Pubitemid 34081178)
    • (2002) Advanced Drug Delivery Reviews , vol.54 , Issue.1 , pp. 3-12
    • Hoffman, A.S.1
  • 94
    • 79955599895 scopus 로고    scopus 로고
    • PH triggered injectable amphiphilic hydrogel containing doxorubicin and paclitaxel
    • Zhao L, Zhu L, Liu F, et al. pH triggered injectable amphiphilic hydrogel containing doxorubicin and paclitaxel. Int J Pharm 2011;410:83-91
    • (2011) Int J Pharm , vol.410 , pp. 83-91
    • Zhao, L.1    Zhu, L.2    Liu, F.3
  • 95
    • 67651180535 scopus 로고    scopus 로고
    • Synergistic anti-tumor activity of paclitaxel-incorporated conjugated linoleic acid-coupled poloxamer thermosensitive hydrogel in vitro and in vivo
    • Guo D, Xu CX, Quan JS, et al. Synergistic anti-tumor activity of paclitaxel-incorporated conjugated linoleic acid-coupled poloxamer thermosensitive hydrogel in vitro and in vivo. Biomaterials 2009;30:4777-85
    • (2009) Biomaterials , vol.30 , pp. 4777-4785
    • Guo, D.1    Xu, C.X.2    Quan, J.S.3
  • 96
    • 84862777576 scopus 로고    scopus 로고
    • Hyaluronic acid-based hydrogel for regional delivery of paclitaxel to intraperitoneal tumors
    • Bajaj G, Kim MR, Mohammed SI, et al. Hyaluronic acid-based hydrogel for regional delivery of paclitaxel to intraperitoneal tumors. J Control Release 2012;158:386-92
    • (2012) J Control Release , vol.158 , pp. 386-392
    • Bajaj, G.1    Kim, M.R.2    Mohammed, S.I.3
  • 97
    • 79958101789 scopus 로고    scopus 로고
    • Multi-responsive nanogels containing motifs of ortho ester, oligo(ethylene glycol) and disulfide linkage as carriers of hydrophobic anti-cancer drugs
    • Qiao ZY, Zhang R, Du FS, et al. Multi-responsive nanogels containing motifs of ortho ester, oligo(ethylene glycol) and disulfide linkage as carriers of hydrophobic anti-cancer drugs. J Control Release 2011;152:57-66
    • (2011) J Control Release , vol.152 , pp. 57-66
    • Qiao, Z.Y.1    Zhang, R.2    Du, F.S.3
  • 98
    • 77957942614 scopus 로고    scopus 로고
    • A strategy for precision engineering of nanoparticles of biodegradable copolymers for quantitative control of targeted drug delivery
    • Liu YT, Li K, Liu B, Feng SS. A strategy for precision engineering of nanoparticles of biodegradable copolymers for quantitative control of targeted drug delivery. Biomaterials 2010;31:9145-55
    • (2010) Biomaterials , vol.31 , pp. 9145-9155
    • Liu, Y.T.1    Li, K.2    Liu, B.3    Feng, S.S.4
  • 99
    • 83555179057 scopus 로고    scopus 로고
    • Quantitative control of targeting effect of anticancer drugs formulated by ligand-conjugated nanoparticles of biodegradable copolymer blend
    • Zhao J, Mi Y, Liu YT, Feng SS. Quantitative control of targeting effect of anticancer drugs formulated by ligand-conjugated nanoparticles of biodegradable copolymer blend. Biomaterials 2012;33:1948-58
    • (2012) Biomaterials , vol.33 , pp. 1948-1958
    • Zhao, J.1    Mi, Y.2    Liu, Y.T.3    Feng, S.S.4
  • 100
    • 84865027076 scopus 로고    scopus 로고
    • Multimodality treatment of cancer with herceptin conjugated, thermomagnetic iron oxides and docetaxel loaded nanoparticles of biodegradable polymers
    • Mi Y, Liu XL, Zhao J, et al. Multimodality treatment of cancer with herceptin conjugated, thermomagnetic iron oxides and docetaxel loaded nanoparticles of biodegradable polymers. Biomaterials 2012;33:7519-29
    • (2012) Biomaterials , vol.33 , pp. 7519-7529
    • Mi, Y.1    Liu, X.L.2    Zhao, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.