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Published on: September 17, 2014
Schizophrenia Treatment Based on Sustained Release of Risperidone from Poly(lactic-co-glycolic) Acid Implantable
Linlin Li1, Li Zhao1, Mingshan Li1
1School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, United Kingdom.
This study introduces a new poly(lactic-co-glycolic) acid microneedle patch for risperidone delivery, offering a self-administered, long-lasting schizophrenia treatment. The patch ensures sustained drug release and therapeutic plasma concentrations, improving patient compliance and reducing medical interventions.
Area of Science:
- Biomedical Engineering
- Materials Science
- Pharmacology
Background:
- Schizophrenia affects 24 million globally, with current treatments like injections having limitations.
- Conventional drug delivery methods for schizophrenia can be painful and require professional administration.
- There is a need for improved drug delivery systems offering sustained release and patient convenience.
Purpose of the Study:
- To develop and evaluate a poly(lactic-co-glycolic) acid (PLGA)-based implantable microneedle patch (IMN) for transdermal risperidone (RIS) delivery.
- To assess the mechanical properties, biocompatibility, and drug release profile of the RIS-loaded IMN.
- To investigate the in vivo efficacy of the RIS IMN in a rat model compared to intramuscular injection.
Main Methods:
- Fabrication of PLGA-based microneedle patches loaded with risperidone.
- Characterization using microscopy, differential scanning calorimetry, and infrared spectroscopy.
- In vitro drug release, ex vivo skin permeation, in vitro cytocompatibility, and in vivo pharmacokinetic studies in rats.
Main Results:
- RIS IMNs exhibited excellent mechanical properties and successful insertion into model skin.
- Biocompatibility studies showed no cytotoxicity to human dermal fibroblasts.
- In vitro studies demonstrated sustained RIS release over 7 days with over 65% delivery efficiency.
- In vivo studies showed sustained therapeutic plasma concentrations for 9 days, outperforming intramuscular injection's short duration.
Conclusions:
- RIS IMNs provide a promising, self-administering transdermal drug delivery system for schizophrenia treatment.
- The developed IMN offers prolonged therapeutic effects and potentially reduces the need for frequent medical interventions.
- This novel approach could significantly improve treatment adherence and patient outcomes in schizophrenia management.
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