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Amphiphilic, lauric acid-coupled pluronic-based nano-micellar system for efficient glipizide delivery.
Kumar, Vipan; Poonia, Neelam; Kumar, Pradeep; Kumar Verma, Prabhakar; Alshammari, Abdulrahman; Albekairi, Norah A; Kabra, Atul; Yadav, Neera.
Afiliación
  • Kumar V; Department of Pharmaceutical Chemistry, JCDM College of Pharmacy, Sirsa 125055, India.
  • Poonia N; Department of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak 124001, India.
  • Kumar P; University Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab, India.
  • Kumar Verma P; Wits Advanced Drug Delivery Platform (WADDP) Research Unit, Department of Pharmacy and Pharmacology, School of Therapeutic Sciences, Faculty of Health Sciences, University of Witwatersrand, 7 York Road, Parktown, Johannesburg 2193, South Africa.
  • Alshammari A; Department of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak 124001, India.
  • Albekairi NA; Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Post Box 2455, Riyadh 11451, Saudi Arabia.
  • Kabra A; Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Post Box 2455, Riyadh 11451, Saudi Arabia.
  • Yadav N; University Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab, India.
Saudi Pharm J ; 32(5): 102046, 2024 May.
Article en En | MEDLINE | ID: mdl-38577487
ABSTRACT
Glipizide; an insulin secretagogue belonging to the sulfonylurea class, is a widely used antidiabetic drug for managing type 2 diabetes. However, the need for life-long administration and repeated doses poses challenges in maintaining optimal blood glucose levels. In this regard, orally active sustained-release nano-formulations can be a better alternative to traditional antidiabetic formulations. The present study explored an innovative approach by formulating orally active sustained-release nano-micelles using the amphiphilic lauric acid-conjugated-F127 (LAF127) block copolymer. LAF127 block copolymer was synthesized through esterification and thoroughly characterized before being employed to develop glipizide-loaded nano-micelles (GNM) via the thin-film hydration technique. The optimized formulation exhibited mean particle size of 341.40 ± 3.21 nm and depicted homogeneous particle size distribution with a polydispersity index (PDI) < 0.2. The formulation revealed a surface charge of -17.11 ± 6.23 mV. The in vitro release studies of glipizide from developed formulation depicted a sustained release profile. Drug loaded micelles exhibited a substantial reduction in blood glucose levels in diabetic rats for a duration of up to 24 h. Notably, neither the blank nano-micelles of LAF127 nor the drug loaded micelles manifested any indications of toxicity in healthy rats. This study provides an insight on suitability of synthesized LAF127 block copolymer for development of effective oral drug delivery systems for anti-diabetic activity without any significant adverse effects.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Saudi Pharm J Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Arabia Saudita

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Saudi Pharm J Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Arabia Saudita