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Dual-responsive in situ gelling polymer matrix for tunable ketamine general anesthesia in experimental animals.
Abd Ellah, Noura H; Helmy, Abdelrahman M; Tammam, Omar Y; El-Sherif, Mohamed W; Abouelmagd, Sara A.
Afiliación
  • Abd Ellah NH; Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt; Department of Pharmaceutics, Faculty of Pharmacy, Badr University in Assiut, Naser City 2014101, Assiut, Egypt.
  • Helmy AM; Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Deraya University, Minya 61768, Egypt; Pharmaceutical Engineering and 3D Printing (PharmE3D) Lab, Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX
  • Tammam OY; Department of Biochemistry, Faculty of Pharmacy, New Valley University, Alkharga, New Valley 72511, Egypt.
  • El-Sherif MW; Department of Surgery, Faculty of Veterinary Medicine, New Valley University, Alkharga, New Valley 72511, Egypt. Electronic address: mohamedelsherif@vet.nvu.edu.eg.
  • Abouelmagd SA; Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt; Institute for Drug Development and Innovation Research, Assiut University, Assiut 71526, Egypt. Electronic address: sabouelm@aun.edu.eg.
Int J Pharm ; 652: 123820, 2024 Mar 05.
Article en En | MEDLINE | ID: mdl-38242258
ABSTRACT
Animal experimentation is a critical part of the drug development process and pharmaceutical research. General anesthesia is one of the most common procedures. Careful administration and dosing of anesthetics ensure animal safety and study success. However, repeated injections are needed to maintain anesthesia, leading to adverse effects. Ketamine, a dissociative anesthetic, is commonly used for inducing anesthesia in animals and suffers from a short half-life requiring repeated dosing. Herein, we report a novel system for controlled anesthesia post-intraperitoneal administration. A polymer solution called "premix" was developed using two stimuli-responsive polymers, Pluronic (PF) and Carbopol (CP). As the premix was mixed with ketamine solution and injected, it underwent in situ gelation, hence controlling ketamine release and anesthesia. The PF and CP concentrations were optimized for the gelation temperature and viscosity upon mixing with the ketamine solution. The optimal premix/ketamine formulation (1.51) was liquid at room temperature and gel at physiological conditions with favorable mucoadhesion and rheology. Premix retarded the release of ketamine, translating to tunable anesthesia in vivo. Anesthesia duration and recovery were tunable per ketamine dose with minimal side effects. Therefore, we propose the implementation of PF/CP premix as a vehicle for general anesthesia in animals for optimal duration and effect.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ketamina Idioma: En Revista: Int J Pharm Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ketamina Idioma: En Revista: Int J Pharm Año: 2024 Tipo del documento: Article