The Metolazone is a diuretic used in the treatment of hypertension and edema. However, its poor aqueous solubility limits its bioavailability and therapeutic efficacy. This study aims to prepare solid lipid nanoparticles (SLNs) loaded with metolazone using an emulsification and low-temperature solidification method and to enhance the solubility and bioavailability of Metolazone through improved formulation techniques. The SLNs were prepared using glyceryl monostearate (GMS) as the lipid matrix, Poloxamer as the surfactant, and lecithin as a stabilizer. The solid lipid nanoparticles (SLNs) were characterized by a particle size, polydispersity index PDI, entrapment efficiency and zeta potential. Characterization of the SLNs included determination of particle size 189.7 nm, polydispersity index PDI of 0.2, high entrapment efficiency 98.26% and zeta potential -21.52 mV. In this study, metolazone–loaded solid lipid nanoparticles were successfully prepared and characterized. Also the bioavailability of Metolazone, a drug with inherently low solubility when administered orally were significantly enhanced.
| Primary Language | English |
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| Subjects | Pharmaceutical Chemistry, Pharmacology and Pharmaceutical Sciences (Other) |
| Journal Section | Articles |
| Authors | |
| Publication Date | November 2, 2025 |
| Submission Date | August 16, 2024 |
| Acceptance Date | November 1, 2024 |
| Published in Issue | Year 2025 Volume: 29 Issue: 6 |