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Twin Screw Melt Granulation: Alternative Approach for Improving Solubility and Permeability of a Non-steroidal Anti-inflammatory Drug Ibuprofen.
Nyavanandi, Dinesh; Narala, Sagar; Mandati, Preethi; Alzahrani, Abdullah; Kolimi, Praveen; Almotairy, Ahmed; Repka, Michael A.
Afiliación
  • Nyavanandi D; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Narala S; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Mandati P; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Alzahrani A; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Kolimi P; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Almotairy A; Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Jackson, MS, 38677, USA.
  • Repka MA; Pharmaceutics and Pharmaceutical Technology Department, College of Pharmacy, Taibah University, AlMunawarah, Al Madinah, 30001, Saudi Arabia.
AAPS PharmSciTech ; 24(1): 47, 2023 Jan 26.
Article en En | MEDLINE | ID: mdl-36703024
The current research is focused on investigating the suitability of the twin screw melt granulation (TSMG) approach for improving the solubility of a non-steroidal anti-inflammatory (NSAIDs) drug (ibuprofen), by developing granules using lipid surfactants. The solubility of the drug within the solid lipid excipients (Gelucire® 48/16 and Gelucire® 50/13) was determined by differential scanning calorimetry (DSC). The formulations were developed for drug and lipid ratios of 1:1.5, 1:3, and 1:4.5 using Neusilin® US2 as a solid adsorbent carrier. The solid-state properties of the drug investigated using differential scanning calorimetry (DSC) have revealed the conversion of the drug to an amorphous form for 1:3 and 1:4.5 ratios of formulations confirmed by powder x-ray diffraction analysis (PXRD). Drug-excipient compatibility and formation of no interactions were characterized using Fourier transform infrared spectroscopy (FTIR). The granules with a 1:3 and 1:4.5 ratios of drug and lipid have improved drug dissolution and permeation, attributing to the formation of micellar emulsions. The stability of formulation with a 1:3 ratio of drug and lipid surfactant was preserved when stored in accelerated conditions. However, the formulation with a 1:4.5 ratio of drug and lipid failed to retain the amorphous state evidenced by the recrystallization of the drug. This shows the suitability of TSMG as a single-step continuous manufacturing process for developing melt granules to improve the solubility of poorly water-soluble drug substances.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antiinflamatorios no Esteroideos / Ibuprofeno Idioma: En Revista: AAPS PharmSciTech Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antiinflamatorios no Esteroideos / Ibuprofeno Idioma: En Revista: AAPS PharmSciTech Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos