دورية أكاديمية

Development and optimization of vildagliptin solid lipid nanoparticles loaded ocuserts for controlled ocular delivery: A promising approach towards treating diabetic retinopathy

التفاصيل البيبلوغرافية
العنوان: Development and optimization of vildagliptin solid lipid nanoparticles loaded ocuserts for controlled ocular delivery: A promising approach towards treating diabetic retinopathy
المؤلفون: Abd El hakim Ramadan, Mahmoud M.A. Elsayed, Amani Elsayed, Marwa A. Fouad, Mohamed S. Mohamed, Sangmin Lee, Reda A. Mahmoud, Shereen A. Sabry, Mohammed M. Ghoneim, Ahmed H.E. Hassan, Reham A. Abd Elkarim, Amany Belal, Ahmed A. El-Shenawy
المصدر: International Journal of Pharmaceutics: X, Vol 7, Iss , Pp 100232- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Pharmacy and materia medica
مصطلحات موضوعية: Diabetic retinopathy, Vildagliptin, Solid lipid nanoparticles, Double emulsion/ melt dispersion technique, Ocuserts, Solvent casting technique, Pharmacy and materia medica, RS1-441
الوصف: Diabetes mellitus (DM) is the most prevalent cause of diabetic retinopathy (DRP). DRP has been recognized for a long time as a microvascular disease. Many drugs were used to treat DRP, including vildagliptin (VLD). In addition to its hypoglycemic effect, VLD minimizes ocular inflammation and improves retinal blood flow for individuals with type 2 diabetes mellitus. Nevertheless, VLD can cause upper respiratory tract infections, diarrhea, nausea, hypoglycemia, and poor tolerability when taken orally regularly due to its high water solubility and permeability. Effective ocular administration of VLD is achieved using solid lipid nanoparticles (SLNPs), which improve corneal absorption, prolonged retention, and extended drug release. Ocuserts (OCUs) are sterile, long-acting ocular dosage forms that diminish the need for frequent dosing while improving residence time and stability. Therefore, this study intends to develop VLD solid lipid nanoparticle OCUs (VLD-SLNPs-OCUs) to circumvent the issues commonly associated with VLD. SLNPs were prepared using the double-emulsion/melt dispersion technique. The optimal formula has been implemented in OCUs. Optimization and development of VLD-SLNPs-OCUs were performed using a Box-Behnken Design (BBD). VLD-SLNPs-OCUs loading efficiency was 95.28 ± 2.87%, and differential scanning calorimetry data (DSC) showed the full transformation of VLD to an amorphous state and the excellent distribution in the prepared OCUs matrices. The in vivo release of VLD from the optimized OCUs after 24 h was 35.12 ± 2.47%, consistent with in vitro drug release data of 36.89 ± 3.11. The optimized OCUs are safe to use in the eye, as shown by the ocular irritation test. VLD-SLNPs-OCUs provide extended VLD release, an advantageous alternative to conventional oral dose forms, resulting in fewer systemic adverse effects and less variation in plasma drug levels. VLD-SLNPs-OCUs might benefit retinal microvascular blood flow beyond blood glucose control and may be considered a promising approach to treating diabetic retinopathy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2590-1567
العلاقة: http://www.sciencedirect.com/science/article/pii/S2590156724000045Test; https://doaj.org/toc/2590-1567Test
DOI: 10.1016/j.ijpx.2024.100232
الوصول الحر: https://doaj.org/article/90e9c3cc813e48a999c5c8078831a32bTest
رقم الانضمام: edsdoj.90e9c3cc813e48a999c5c8078831a32b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25901567
DOI:10.1016/j.ijpx.2024.100232