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Volumn 5, Issue 3, 2002, Pages 30-35

Lipid-based oral dosage forms - Regulatory perspective

(1)  Chen, Mei Ling a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACYLTRANSFERASE; ALCOHOL DEHYDROGENASE; ALDEHYDE DEHYDROGENASE; CATECHOL METHYLTRANSFERASE; CYCLOSPORIN; CYCLOSPORIN A; CYTOCHROME P450; DIHYDROPYRIMIDINE DEHYDROGENASE; DRUG VEHICLE; EPOXIDE HYDROLASE; ESTERASE; GLUCURONOSYLTRANSFERASE; GLUTATHIONE TRANSFERASE; GLYCOPROTEIN P; HISTAMINE METHYLTRANSFERASE; LIPID; NEW DRUG; OXIDOREDUCTASE; SAQUINAVIR; SULFOTRANSFERASE; THIOPURINE METHYLTRANSFERASE; TOCOFERSOLAN; URIDINE TRIPHOSPHATE;

EID: 0036742042     PISSN: 10998012     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (16)
  • 1
    • 0035007337 scopus 로고    scopus 로고
    • Formulation and physiological and biopharmaceutical issues in the development of oral lipid-based drug delivery systems
    • K. M. Wasan. Formulation and physiological and biopharmaceutical issues in the development of oral lipid-based drug delivery systems. Drug Develop. Indust. Pharm. 27:267-276 (2001).
    • (2001) Drug Develop. Indust. Pharm , vol.27 , pp. 267-276
    • Wasan, K.M.1
  • 2
    • 0033812424 scopus 로고    scopus 로고
    • Lipids, lipophilic drugs, and oral drug delivery - Some emerging concepts
    • W. N. Charman. Lipids, lipophilic drugs, and oral drug delivery -Some emerging concepts. J. Pharm. Sci. 89:967-978 (2000).
    • (2000) J. Pharm. Sci , vol.89 , pp. 967-978
    • Charman, W.N.1
  • 3
    • 0029562489 scopus 로고
    • Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects
    • P. P. Constantinides. Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects. Pharm. Res. 12:1561-1572 (1995).
    • (1995) Pharm. Res , vol.12 , pp. 1561-1572
    • Constantinides, P.P.1
  • 4
    • 0025882648 scopus 로고
    • Microemulsions for improved peptide absorption from the gastrointestinal tract
    • W. A. Ritschel. Microemulsions for improved peptide absorption from the gastrointestinal tract. Meth. Find. Exp. Clin. Pharmacol. 13:205-220 (1993).
    • (1993) Meth. Find Exp. Clin. Pharmacol , vol.13 , pp. 205-220
    • Ritschel, W.A.1
  • 5
    • 0033849510 scopus 로고    scopus 로고
    • Preparation of biodegradable insulin nanocapsules from biocompatible microemulsion
    • S. Watnasirichaikul, N. M. Davies, T. Rades and I. G. Tucker. Preparation of biodegradable insulin nanocapsules from biocompatible microemulsion. Pharm. Res. 17:684-689 (2000).
    • (2000) Pharm. Res , vol.17 , pp. 684-689
    • Watnasirichaikul, S.1    Davies, N.M.2    Rades, T.3    Tucker, I.G.4
  • 6
    • 4243572311 scopus 로고    scopus 로고
    • Challenges in the development of lipid-based formulations
    • AAPS Pharmaceutics and Drug Delivery Conference, Arlington, VA. April
    • R. Roman. Challenges in the development of lipid-based formulations. AAPS Pharmaceutics and Drug Delivery Conference, Arlington, VA. April 22-24, 2002.
    • (2002) , pp. 22-24
    • Roman, R.1
  • 7
    • 0010537821 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-- General Considerations, Office of Training and Communicat
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-- General Considerations, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville MD 20857, October 2000.
    • (2000)
  • 8
    • 0010537552 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate Release Solid Oral Dosage Forms Based on a Biopharmaceutics Class
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville MD 20857, August 2000.
    • (2000)
  • 9
    • 0010539393 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations, Office of Training and Commun
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville MD 20857, September 1997.
    • (1997)
  • 10
    • 0010539111 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms, Office of Training and Communications, Division of Communications Manageme
    • U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville MD 20857, August 1997.
    • (1997)
  • 11
    • 0031891234 scopus 로고    scopus 로고
    • Triglyceride-based microemulsion for intravenous administration of sparingly soluble substances
    • C. von Corswant, P. Thoren and S. Engstrom. Triglyceride-based microemulsion for intravenous administration of sparingly soluble substances. J. Pharm. Sci. 87:200-208 (1998).
    • (1998) J. Pharm. Sci , vol.87 , pp. 200-208
    • von Corswant, C.1    Thoren, P.2    Engstrom, S.3
  • 12
    • 0033051406 scopus 로고    scopus 로고
    • A new method for dissolution studies of Lipid-filled capsules employing nifedipine as a model drug
    • V. Pillay and R. Fassihi. A new method for dissolution studies of Lipid-filled capsules employing nifedipine as a model drug. Pharm. Res. 16:333-337 (1999).
    • (1999) Pharm. Res , vol.16 , pp. 333-337
    • Pillay, V.1    Fassihi, R.2
  • 13
    • 0010609267 scopus 로고    scopus 로고
    • U. S. Pharmacopeia 25/National Formulary 20, General Chapters, Physical Tests and Determinations, <711> Dissolution
    • U. S. Pharmacopeia 25/National Formulary 20, General Chapters, Physical Tests and Determinations, <711> Dissolution, p. 2011 (2002).
    • (2002) , pp. 2011
  • 14
    • 0029925318 scopus 로고    scopus 로고
    • The effect of water-soluble vitamin E on cyclosporine pharmacokinetics in healthy volunteers
    • T. Chang, L. Z. Benet and M. F. Hebert. The effect of water-soluble vitamin E on cyclosporine pharmacokinetics in healthy volunteers. Clin. Pharmacol. Ther. 59:297-303 (1996).
    • (1996) Clin. Pharmacol. Ther , vol.59 , pp. 297-303
    • Chang, T.1    Benet, L.Z.2    Hebert, M.F.3
  • 15
    • 0028335905 scopus 로고
    • Reduced inter- and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation
    • J. M. Kovarik, E. A. Mueller, J. B. van Bree, W. Tetzloff and K. Kutz. Reduced inter- and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation. J. Pharm. Sci. 83:444-446 (1994).
    • (1994) J. Pharm. Sci , vol.83 , pp. 444-446
    • Kovarik, J.M.1    Mueller, E.A.2    van Bree, J.B.3    Tetzloff, W.4    Kutz, K.5
  • 16
    • 0034644369 scopus 로고    scopus 로고
    • Nationwide recall of SangCya oral solution
    • J. E. Henney. Nationwide recall of SangCya oral solution. JAMA, 284(10):1234 (2000).
    • (2000) JAMA , vol.284 , Issue.10 , pp. 1234
    • Henney, J.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.