Formulation, In-Vitro and In-Vivo Evaluation of Lamivudine-Loaded Solid Lipid Nanoparticles (SLNs)
Background: The solubility and permeability of drugs could be improved using lipid based drug delivery systems (LBDDS). Drugs are usually classified into four groups according to Biopharmaceutical classification system. Lamivudine is a class 3 drug with high solubility and low permeability.
Objectives: Lamivudine-loaded solid lipid particles were formulated and evaluated using different lipid matrices consisting of phospholipon 90H® and softisan® 154 in the ratio of 1:2, and in-vitro and in-vivo characterizations were done on solid-lipid nanoparticles (SLNs).
Materials/Method: Fusion method was used in the preparation of the lipid matrices using mixtures of phospholipon® 90H and softisan® 154 in the ratio of 1:2. They were melted together in a crucible using a water bath and subsequently stirred with a glass stirrer at 70 oC to get a homogenous transparent yellow melt. The homogenous mixture was subsequently stirred at room temperature to get solidification.
Results: The pH range of the batches formulated with lipid ratio 1:2 was 4.9. After 3 months interval, there was no significant change in pH of the formulated SLNs, which resulted in no significant degradation of the drug and excipients that were used in the formulation. The encapsulation efficiency (EE) of batch F1 was 84 %, while batches F2 and F3 were 75 % and 71 % respectively. Loading capacity for the three batches F1, F2 and F3 were 4.2 %, 7.5 % and 14.2 % respectively. The release studies obtained showed that the SLN had a percentage drug release of 63.5 % to 72.8 % after 10 h in simulated intestinal fluid (SIF) while in simulated gastric fluid (SGF), the percentage drug release was 49 % to 60 %. The in-vitro result obtained, showed that batch P (Pure standard lamivudine) recorded increased CD4+ count from day 0 to 21, while batch N (control) showed no sign of CD4+ count depletion.
Conclusion: The method was used successfully.
Download the full article as PDF here: Formulation, In-Vitro and In-Vivo Evaluation of Lamivudine Loaded Solid Lipid Nanoparticles (SLNs)
Materials
Phospholipon 90H (Phospholipid GmbH, Koln, Germany), Softisan 154® (Schuppen Chondea, chemei, GmbH, Germany), Sorbic acid (Sigma Chemical company, USA), Tween 80 (Sigma Chemical company, USA), Sorbitol (Wharfedale laboratories, Otley, UK), Monobasic potassium phosphate (Sigma Chemical company, USA), Sodium hydroxide (Sigma Chemical company, USA), distilled water (UNN Water Resources, Nsukka, Nigeria), Lamivudine (Paucocyclo, Kwality Pharmaceuticals, India).
Chime AS, et al. (2024). Formulation, In-Vitro and In-Vivo Evaluation of LamivudineLoaded Solid Lipid Nanoparticles (SLNs). Mathews J Pharma Sci. 8(1):28.
Looking for small(er) to medium production quantaties of excipients?
Read more on EXCIPIO CHEMICALS here:
