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Volumn 478, Issue 2, 2015, Pages 718-725

Sylysia 350/Eudragit S100 solid nanomatrix as a promising system for oral delivery of cyclosporine A

Author keywords

Bioavailability; Cyclosporine A; Nanomatrix; pH sensitive delivery system; Poorly soluble drug

Indexed keywords

CYCLOSPORIN A; DRUG VEHICLE; EUDRAGIT; EXCIPIENT; SILICON DIOXIDE; SYLYSIA 350; UNCLASSIFIED DRUG; CYCLOSPORIN; IMMUNOSUPPRESSIVE AGENT; METHYLMETHACRYLATE-METHACRYLIC ACID COPOLYMER; NANOMATERIAL; POLYMETHACRYLIC ACID DERIVATIVE; AEROSIL; CYCLOSPORIN D; NANOCARRIER; NANOPARTICLE; SILICA NANOPARTICLE;

EID: 84919667612     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2014.11.030     Document Type: Article
Times cited : (25)

References (21)
  • 1
    • 3242673239 scopus 로고    scopus 로고
    • PH-sensitive nanoparticles for improving the oral bioavailability of cyclosporine A
    • J. Dai, T. Nagai, X. Wang, T. Zhang, M. Meng, and Q. Zhang pH-sensitive nanoparticles for improving the oral bioavailability of cyclosporine A Int. J. Pharm. 280 2004 229 240
    • (2004) Int. J. Pharm. , vol.280 , pp. 229-240
    • Dai, J.1    Nagai, T.2    Wang, X.3    Zhang, T.4    Meng, M.5    Zhang, Q.6
  • 2
    • 0026567874 scopus 로고
    • The absorption site of cyclosporin in the human gastrointestinal tract
    • J. Drewe, C. Beglinger, and T. Kissel The absorption site of cyclosporin in the human gastrointestinal tract Br. J. Clin. Pharmacol. 33 1992 39 43
    • (1992) Br. J. Clin. Pharmacol. , vol.33 , pp. 39-43
    • Drewe, J.1    Beglinger, C.2    Kissel, T.3
  • 3
    • 0035238531 scopus 로고    scopus 로고
    • Cyclosporin: An updated review of the pharmacokinetic properties, clinical efficacy and tolerability of a microemulsion-based formulation (neoral) 1 in organ transplantation
    • C.J. Dunn, A.J. Wagstaff, C.M. Perry, G.L. Plosker, and K.L. Goa Cyclosporin: an updated review of the pharmacokinetic properties, clinical efficacy and tolerability of a microemulsion-based formulation (neoral) 1 in organ transplantation Drugs 61 2001 1957 2016
    • (2001) Drugs , vol.61 , pp. 1957-2016
    • Dunn, C.J.1    Wagstaff, A.J.2    Perry, C.M.3    Plosker, G.L.4    Goa, K.L.5
  • 4
    • 80155182416 scopus 로고    scopus 로고
    • Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt
    • P. Guan, Y. Lu, J. Qi, M. Niu, R. Lian, F. Hu, and W. Wu Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt Int. J. Nanomed. 6 2011 965 974
    • (2011) Int. J. Nanomed. , vol.6 , pp. 965-974
    • Guan, P.1    Lu, Y.2    Qi, J.3    Niu, M.4    Lian, R.5    Hu, F.6    Wu, W.7
  • 5
    • 70349303554 scopus 로고    scopus 로고
    • Improvement of cyclosporine A bioavailability by incorporating ethyl docosahexaenoate in the microemulsion as an oil excipient
    • V. Hirunpanich, and H. Sato Improvement of cyclosporine A bioavailability by incorporating ethyl docosahexaenoate in the microemulsion as an oil excipient Eur. J. Pharm. Biopharm.: Off. J. Arbeitsgemeinschaft Pharm. Verfahrenstechnik e.V 73 2009 247 252
    • (2009) Eur. J. Pharm. Biopharm.: Off. J. Arbeitsgemeinschaft Pharm. Verfahrenstechnik E.V , vol.73 , pp. 247-252
    • Hirunpanich, V.1    Sato, H.2
  • 7
    • 77951189574 scopus 로고    scopus 로고
    • Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles
    • J. Lai, Y. Lu, Z. Yin, F. Hu, and W. Wu Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles Int. J. Nanomed. 5 2010 13 23
    • (2010) Int. J. Nanomed. , vol.5 , pp. 13-23
    • Lai, J.1    Lu, Y.2    Yin, Z.3    Hu, F.4    Wu, W.5
  • 8
    • 84862291314 scopus 로고    scopus 로고
    • Solid self-nanoemulsifying cyclosporine A pellets prepared by fluid-bed coating: Stability and bioavailability study
    • Y. Lei, J. Qi, S. Nie, F. Hu, W. Pan, Y. Lu, and W. Wu Solid self-nanoemulsifying cyclosporine A pellets prepared by fluid-bed coating: stability and bioavailability study J. Biomed. Nanotechnol. 8 2012 515 521
    • (2012) J. Biomed. Nanotechnol. , vol.8 , pp. 515-521
    • Lei, Y.1    Qi, J.2    Nie, S.3    Hu, F.4    Pan, W.5    Lu, Y.6    Wu, W.7
  • 11
    • 33744973517 scopus 로고    scopus 로고
    • Oral bioavailability of cyclosporine: Solid lipid nanoparticles (SLN) versus drug nanocrystals
    • R.H. Muller, S. Runge, V. Ravelli, W. Mehnert, A.F. Thunemann, and E.B. Souto Oral bioavailability of cyclosporine: solid lipid nanoparticles (SLN) versus drug nanocrystals Int. J. Pharm. 317 2006 82 89
    • (2006) Int. J. Pharm. , vol.317 , pp. 82-89
    • Muller, R.H.1    Runge, S.2    Ravelli, V.3    Mehnert, W.4    Thunemann, A.F.5    Souto, E.B.6
  • 12
    • 77956880320 scopus 로고    scopus 로고
    • Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach
    • S. Onoue, H. Sato, K. Ogawa, Y. Kawabata, T. Mizumoto, K. Yuminoki, N. Hashimoto, and S. Yamada Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach Int. J. Pharm. 399 2010 94 101
    • (2010) Int. J. Pharm. , vol.399 , pp. 94-101
    • Onoue, S.1    Sato, H.2    Ogawa, K.3    Kawabata, Y.4    Mizumoto, T.5    Yuminoki, K.6    Hashimoto, N.7    Yamada, S.8
  • 16
    • 15044343842 scopus 로고    scopus 로고
    • Solid dispersion particles of amorphous indomethacin with fine porous silica particles by using spray-drying method
    • H. Takeuchi, S. Nagira, H. Yamamoto, and Y. Kawashima Solid dispersion particles of amorphous indomethacin with fine porous silica particles by using spray-drying method Int. J. Pharm. 293 2005 155 164
    • (2005) Int. J. Pharm. , vol.293 , pp. 155-164
    • Takeuchi, H.1    Nagira, S.2    Yamamoto, H.3    Kawashima, Y.4
  • 18
    • 0032990165 scopus 로고    scopus 로고
    • Modification of release rates of cyclosporin A from polyl(l-lactic acid) microspheres by fatty acid esters and in-vivo evaluation of the microspheres
    • T. Urata, K. Arimori, and M. Nakano Modification of release rates of cyclosporin A from polyl(l-lactic acid) microspheres by fatty acid esters and in-vivo evaluation of the microspheres J. Controlled Release 58 1999 133 141
    • (1999) J. Controlled Release , vol.58 , pp. 133-141
    • Urata, T.1    Arimori, K.2    Nakano, M.3
  • 20
    • 60449112985 scopus 로고    scopus 로고
    • Controllable release of ibuprofen from size-adjustable and surface hydrophobic mesoporous silica spheres
    • W. Xu, Q. Gao, Y. Xu, D. Wu, Y. Sun, W. Shen, and F. Deng Controllable release of ibuprofen from size-adjustable and surface hydrophobic mesoporous silica spheres Powder Technol. 191 2009 13 20
    • (2009) Powder Technol. , vol.191 , pp. 13-20
    • Xu, W.1    Gao, Q.2    Xu, Y.3    Wu, D.4    Sun, Y.5    Shen, W.6    Deng, F.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.