Schizophrenia Treatment Based on Sustained Release of Risperidone from Poly(lactic-<i>co</i>-glycolic) Acid Implantable Microarray Patch
Schizophrenia is one of the most severe mental disorders, affecting approximately 24 million people worldwide. Conventional treatments, such as drug-loaded implants and intramuscular injections, have several limitations, including pain during administration and the need for medical professionals to perform the procedure. In this study, a poly(lactic-<i>co</i>-glycolic) acid (PLGA)-based implantable microneedle patch (IMN) was developed for the transdermal delivery of risperidone (RIS) as a treatment for schizophrenia. RIS IMNs were prepared by sequentially casting gel-based formulations into microneedle (MN) molds. The patches were then characterized using microscopy, differential scanning calorimetry, and infrared spectroscopy, as well as through evaluations of MN insertion and RIS release. A selected formulation was further tested by evaluating its cytocompatibility and its ability to deliver RIS in a rat animal model. The RIS IMN demonstrated excellent mechanical properties, successfully inserting up to 378 nm into model skin, which is crucial for effective transdermal drug delivery. A biocompatibility study using human dermal fibroblasts showed no cytotoxicity, with cell viability and proliferation being close to 100%. The optimized formulation achieved a sustained <i>in vitro</i> release over 7 days, while <i>ex vivo</i> skin deposition and permeation studies showed over 65% RIS delivery efficiency. <i>In vivo</i> animal studies confirmed that RIS IMNs maintained therapeutic plasma concentrations throughout the nine-day experiment, with <i>C</i><sub>max</sub> values of RIS and 9-OH RIS reaching 387.96 ± 194.02 and 139.89 ± 47.68 ng/mL at 6 and 96 h, respectively. In contrast, intramuscular injection showed a <i>C</i><sub>max</sub> of 1756.70 ± 246.06 and 1377.38 ± 160.78 ng/mL at 2 and 6 h but lost therapeutic effect after just 24 h. These findings suggest that RIS IMNs offer significant clinical benefits for patients with schizophrenia, providing prolonged therapeutic effects with a simple, self-administering drug delivery system, reducing the need for frequent medical interventions.
Authors
- Eneko Larrañeta (ORCID: https://orcid.org/0000-0003-3710-0438)
- Natalia Moreno‐Castellanos (ORCID: https://orcid.org/0000-0003-2481-3164)
- Rand Ghanma (ORCID: https://orcid.org/0000-0002-6291-0507)
- Brett Greer (ORCID: https://orcid.org/0000-0001-5039-0244)
- Li Zhao (ORCID: https://orcid.org/0000-0002-5799-6799)
- Ryan F. Donnelly (ORCID: https://orcid.org/0000-0002-0766-4147)
- Akmal Hidayat Bin Sabri (ORCID: https://orcid.org/0000-0002-6698-0393)
- Qonita Kurnia Anjani (ORCID: https://orcid.org/0000-0002-4809-550X)
- Helen O. McCarthy (ORCID: https://orcid.org/0000-0002-1254-3745)
- Linlin Li (ORCID: https://orcid.org/0000-0003-1041-4533)
- Mingshan Li (ORCID: https://orcid.org/0000-0002-5194-500X)
- Yushi Tao
Institutions
- Universidad Industrial de Santander (CO)
- Queen's University Belfast (GB)
- Jordan University of Science and Technology (JO)
- Pharmaceutical Biotechnology (Czechia) (CZ)
Publication Details
- Journal
- ACS Applied Materials & Interfaces
- Published
- 2025-03-06
- DOI
- https://doi.org/10.1021/acsami.4c20010
- Citations
- 6
- Primary Topic
- Advancements in Transdermal Drug Delivery
- Type
- article
- Field-Weighted Citation Impact
- 4.74
Funders
- Engineering and Physical Sciences Research Council