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Gastroretentive Superporous Hydrogel Tablets-Esomeprazole - Srinivasa Rao Yarguntla - Bog

Gastroretentive Superporous Hydrogel Tablets-Esomeprazoleaf Srinivasa Rao Yarguntla
Bag om Gastroretentive Superporous Hydrogel Tablets-Esomeprazole

All the formulations were prepared by direct compression method. The prepared tablets of all the formulations were evaluated for physical characters, assay, in¿vitro drug release, swelling index, hardness and friability. The main aim was to optimize the formulation for 1-12 hours in¿vitro release. Optimized formulation F9 containing chitosan and xanthan gum in 1:1 ratio shows better drug release up to 12hours was consider as the best product with respect to in-vitro drug release for 12 hours release action and improved site¿specific action. The results showed that the drug release rate was decreased as the viscosity of the polymer was increased. The drug release kinetics was performed for the optimized formulation and it shows zero order with super case II transport drug release.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9786206789949
  • Indbinding:
  • Paperback
  • Sideantal:
  • 96
  • Udgivet:
  • 22. oktober 2023
  • Størrelse:
  • 150x6x220 mm.
  • Vægt:
  • 161 g.
  • 2-3 uger.
  • 5. december 2024
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  • BLACK NOVEMBER

Medlemspris

Prøv i 30 dage for 45 kr.
Herefter fra 79 kr./md. Ingen binding.

Beskrivelse af Gastroretentive Superporous Hydrogel Tablets-Esomeprazole

All the formulations were prepared by direct compression method. The prepared tablets of all the formulations were evaluated for physical characters, assay, in¿vitro drug release, swelling index, hardness and friability. The main aim was to optimize the formulation for 1-12 hours in¿vitro release. Optimized formulation F9 containing chitosan and xanthan gum in 1:1 ratio shows better drug release up to 12hours was consider as the best product with respect to in-vitro drug release for 12 hours release action and improved site¿specific action. The results showed that the drug release rate was decreased as the viscosity of the polymer was increased. The drug release kinetics was performed for the optimized formulation and it shows zero order with super case II transport drug release.

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