Literature DB >> 11451031

Once-a-day oral dosing regimen of cyclosporin A: combined therapy of cyclosporin A premicroemulsion concentrates and enteric coated solid-state premicroemulsion concentrates.

C K Kim1, H J Shin, S G Yang, J H Kim, Y K Oh.   

Abstract

PURPOSE: To develop once-a-day oral dosing regimen that provides the blood levels of cyclosporin A (CsA) in the therapeutic ranges over 24 hours.
METHODS: CsA premicroemulsion concentrates (preME) were formulated from phase diagrams. Enteric-coated solid-state premicroemulsion concentrates (sME) were prepared by coating preME with enteric-coating matrials and solidifying them. CsA was measured using high-performance liquid chromatography or radioimmunoassay.
RESULTS: PreME consisted of CsA, oil, and mixture of surfactants and a cosurfactant. PreME spontaneously formed microemulsions in aqueous medium and showed oral absorption profiles similar to Sandimmune Neoral in dogs. Dispersion of sME in aqueous medium also formed microemulsions. Release rates of CsA from sME depended on pH and the type of enteric-coating materials and highly correlated with the extent of oral absorption. The co-administration of preME and sME (200 mg CsA) showed the maximum blood level of CsA not significantly different from that of preME (100 mg CsA) and the concentration of CsA close to the minimum therapeutic level at 24 hours.
CONCLUSIONS: The combined treatment of preME and sME provided controlled oral absorption of CsA over a 24-hour period. Such once-a-day dosing regimens will lead to increased patient compliance and reduced episodes of organ rejection after transplantation.

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Year:  2001        PMID: 11451031     DOI: 10.1023/a:1011046109078

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  14 in total

Review 1.  Renal toxicity of long-term cyclosporin.

Authors:  H Zachariae
Journal:  Scand J Rheumatol       Date:  1999       Impact factor: 3.641

2.  Pharmacodynamic and pharmacokinetic rationales for the development of an oral controlled-release amoxicillin dosage form.

Authors:  A Hoffman; H D Danenberg; I Katzhendler; R Shuval; D Gilhar; M Friedman
Journal:  J Control Release       Date:  1998-06       Impact factor: 9.776

Review 3.  Cyclosporine neurotoxicity: a review.

Authors:  J M Gijtenbeek; M J van den Bent; C J Vecht
Journal:  J Neurol       Date:  1999-05       Impact factor: 4.849

4.  Reduced inter- and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation.

Authors:  J M Kovarik; E A Mueller; J B van Bree; W Tetzloff; K Kutz
Journal:  J Pharm Sci       Date:  1994-03       Impact factor: 3.534

5.  Cyclosporine microemulsion increases drug exposure and reduces acute rejection without incremental toxicity in de novo renal transplantation. International Sandimmun Neoral Study Group.

Authors:  P Keown; D Niese
Journal:  Kidney Int       Date:  1998-09       Impact factor: 10.612

Review 6.  Optimization of cyclosporine therapy in renal transplantation by a pharmacokinetic strategy.

Authors:  B D Kahan; J Grevel
Journal:  Transplantation       Date:  1988-11       Impact factor: 4.939

7.  A randomized, prospective multicenter pharmacoepidemiologic study of cyclosporine microemulsion in stable renal graft recipients. Report of the Canadian Neoral Renal Transplantation Study Group.

Authors:  P Keown; D Landsberg; P Halloran; A Shoker; D Rush; J Jeffery; D Russell; C Stiller; N Muirhead; E Cole; L Paul; J Zaltzman; R Loertscher; P Daloze; R Dandavino; A Boucher; P Handa; J Lawen; P Belitsky; P Parfrey
Journal:  Transplantation       Date:  1996-12-27       Impact factor: 4.939

8.  The absorption site of cyclosporin in the human gastrointestinal tract.

Authors:  J Drewe; C Beglinger; T Kissel
Journal:  Br J Clin Pharmacol       Date:  1992-01       Impact factor: 4.335

Review 9.  Adverse reactions and interactions of cyclosporin.

Authors:  J P Scott; T W Higenbottam
Journal:  Med Toxicol Adverse Drug Exp       Date:  1988 Mar-Apr

Review 10.  Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects.

Authors:  P P Constantinides
Journal:  Pharm Res       Date:  1995-11       Impact factor: 4.200

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2.  Extended release felodipine self-nanoemulsifying system.

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