skip to main content
Tipo de recurso Mostra resultados com: Mostra resultados com: Índice

In vitro release of mitomycin C from collagen implants

Zimmermann, C. ; Drewe, J. ; Flammer, J. ; Shaarawy, T.

Current eye research, 2004, Vol.28 (1), p.1-4 [Periódico revisado por pares]

England: Informa UK Ltd

Texto completo disponível

Citações Citado por
  • Título:
    In vitro release of mitomycin C from collagen implants
  • Autor: Zimmermann, C. ; Drewe, J. ; Flammer, J. ; Shaarawy, T.
  • Assuntos: Animals ; Aqueous Humor - metabolism ; Chromatography, High Pressure Liquid ; Collagen - metabolism ; Drug Carriers ; Half-Life ; Implants, Experimental ; Mitomycin - pharmacokinetics ; Sclera - metabolism ; Sodium Chloride - metabolism ; Swine
  • É parte de: Current eye research, 2004, Vol.28 (1), p.1-4
  • Notas: ObjectType-Article-1
    SourceType-Scholarly Journals-1
    ObjectType-Feature-2
    content type line 23
  • Descrição: Purpose. To study Mitomycin C Loaded Collagen Implant (CI) pharmacokinetics behaviour in vitro. Methods. The CI were incubated for 15 minutes in different MMC loading solutions with the following concentrations: 0.03 mg/mL (n = 9), 0.3 mg/mL (n = 10) and 3.0mg/mL (n = 10). The loaded CI were transferred in 100µL of 0.9% NaCl. Aqueous flow of 5µL/min was simulated. The MMC concentrations of the samples were determined by high performance liquid chromatography (HPLC). Dissolution kinetics were evaluated by a first-order process. The half-life of dissolution and the time of 95% dissolution were determined. Results. The CI absorbed on average a MMC dose of 0.054, 0.530 and 6.090µg when incubated in the different MMC loading solutions containing 0.03 mg/mL, 0.3mg/mL, 3.0 mg/mL of MMC, respectively. In the release experiments, the mean total dose delivered by CI was 0.0493, 0.585 and 5.291µg. A linear correlation between loading concentration and the estimated total dose released was demonstrated. The kinetic parameters showed a fast MMC dissolution. The half-life of the 3 series was 8.8, 10.1 and 10.5 min. Conclusions. Commercially available CI can be loaded with MMC, and could provide relatively slower release than sponge delivery of MMC. Clinical implications of these results warrants further studies.
  • Editor: England: Informa UK Ltd
  • Idioma: Inglês

Buscando em bases de dados remotas. Favor aguardar.