Literature DB >> 27484834

Spontaneous temperature-sensitive Pluronic(®) based niosomes: Triggered drug release using mild hyperthermia.

Lorena Tavano1, Cesare Oliviero Rossi2, Nevio Picci1, Rita Muzzalupo3.   

Abstract

Inclusion of lipids or polymers with a transition temperature closer to physiological body temperature (40-42°C) is a strategy used in tumor therapy for more than 30 years, because it allows induction of drug release from delivery systems by mild hyperthermia. Unfortunately, most of these thermo-sensitive carriers are removed from circulation before completion of their function. Thus, novel multi-functional niosomes possessing spontaneous stealth and thermo-sensitive properties were developed from L64 Pluronic(®) and L64ox as its derivative, in presence or absence of cholesterol. The use of L64 both as amphiphilic constituent and thermo-sensitive molecule, gave the possibility to bypass the use of additional excipients and increased the system biocompatibility. Niosomes diameter ranged from 400 to 750nm and were long term stable. Calcein and 5-FU possess great affinity to niosomal matrices rich in PEO groups. Negative Z-potential values were attributed to the negative charges onto the niosomes surface and generally change according to the temperature. The in vitro drugs release studies were performed at 25°C, 37°C and 42°C, that are representative of certain conditions (storage, physiological condition and mild hyperthermia, respectively). Results showed that L64-based niosomes possess spontaneous thermo-sensitive properties: drugs releases were found to be more pronounced at 42°C. These early results are a promising first step for the development of multi-functional devices that combine several advantages such as stealth properties and temperature controllability at the desired location and time, for a more specific and efficient pharmacological therapy.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Drug release; Hyperthermia; Niosomes; Pluronic(®); Thermo-sensitivity

Mesh:

Substances:

Year:  2016        PMID: 27484834     DOI: 10.1016/j.ijpharm.2016.07.064

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  4 in total

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Authors:  Hongshu Bi; Jianxiu Xue; Hong Jiang; Shan Gao; Dongjuan Yang; Yan Fang; Kai Shi
Journal:  Asian J Pharm Sci       Date:  2018-10-31       Impact factor: 6.598

Review 2.  Nanoarchitectonics of Multifunctional Niosomes for Advanced Drug Delivery.

Authors:  Denitsa B Momekova; Viliana E Gugleva; Petar D Petrov
Journal:  ACS Omega       Date:  2021-12-06

Review 3.  Current Advances in Specialised Niosomal Drug Delivery: Manufacture, Characterization and Drug Delivery Applications.

Authors:  Bwalya A Witika; Kokoette E Bassey; Patrick H Demana; Xavier Siwe-Noundou; Madan S Poka
Journal:  Int J Mol Sci       Date:  2022-08-26       Impact factor: 6.208

Review 4.  Thermo-Sensitive Vesicles in Controlled Drug Delivery for Chemotherapy.

Authors:  Elisabetta Mazzotta; Lorena Tavano; Rita Muzzalupo
Journal:  Pharmaceutics       Date:  2018-09-05       Impact factor: 6.321

  4 in total

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