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Phytochemical Analysis, Antinociceptive and Anti-inflammatory Activities of Mimusops elengi Bojer Leaf Extract-loaded Chitosan Nanoparticles in Albino Mice Ukwubile, Cletus Anes; Clement, Chidi Kaosi
Sciences of Phytochemistry Volume 5 Issue 1
Publisher : ETFLIN

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.58920/sciphy0501490

Abstract

The present study evaluated the antinociceptive and anti-inflammatory activities of Mimusops elengi Bojer leaf extract encapsulated in chitosan nanoparticles (CS-NPs) using murine models, to determine whether nanoparticle formulation enhances the biological effects of a methanolic plant extract. Preliminary phytochemical screening was conducted using established qualitative colorimetric assays, which indicated the presence of major secondary metabolite classes, including phenolics and flavonoids; these tests were intended for compositional inference rather than definitive compound identification. Total phenolic and flavonoid contents were subsequently quantified using spectrophotometric methods, yielding 806.12 mg gallic acid equivalents (GAE)/g and 103.08 mg quercetin equivalents (QE)/g of extract, respectively. Antinociceptive activity was assessed using acetic acid–induced writhing and hot-plate assays, while anti-inflammatory effects were evaluated via the carrageenan-induced paw edema model. Animals treated with M. elengi–loaded CS-NPs exhibited statistically significant reductions in writhing responses, prolonged pain reaction latency, and decreased paw edema when compared with untreated controls and animals receiving the crude extract (p < 0.05). Inflammatory mediator analysis further demonstrated significant downregulation of pro-inflammatory cytokines (TNF-α, IL-1β, and PGE₂) alongside upregulation of anti-inflammatory cytokines (IL-10 and IL-22). Oxidative stress assessment showed reduced malondialdehyde (MDA) levels, indicating attenuation of lipid peroxidation. All experiments were conducted with appropriate replication, and data were subjected to statistical analysis to ensure reproducibility. While the phytochemical screening provides preliminary compositional insights, the observed pharmacological effects are attributed to the combined action of extract constituents and improved delivery via chitosan nanoparticles. Overall, the findings support the hypothesis that nanoparticle-based formulation can enhance the antinociceptive and anti-inflammatory efficacy of M. elengi leaf extract, highlighting its potential as a complementary therapeutic approach while underscoring the need for further compound-level characterization and safety evaluation.
Formulation and Pharmaceutical Evaluation of Capsules Containing the n-Hexane Fraction of Moringa oleifera Leaves Mathias, Sylvester Nefai; Ahmed, Aliyu Hamidu; Mshelia, Emmanuel Halilu; Mohammed, Achor; Ugwah-Oguejiofor, Chinenye Jane; Lawal, Mansur; Alkali, Ibrahim Yusuf; Igbokwe, Nkeiruka Nkeonyere; Ukwubile, Cletus Anes; Biambo, Ahmed Aminu
Sciences of Phytochemistry Volume 5 Issue 1
Publisher : ETFLIN

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.58920/sciphy0501561

Abstract

This study investigated the phytochemical composition, safety profile, and pharmaceutical formulation of capsules containing the hexane fraction of Moringa oleifera leaves (MOHx). The main objective of this study was to comprehensively evaluate the phytochemical constituents, toxicity profile, and develop a standardized oral capsule formulation of the hexane fraction of M. oleifera leaves suitable for potential therapeutic application. Phytochemical profiling was performed using LC–MS and GC–MS, and compounds were tentatively identified based on spectral library matching and fragmentation patterns. Selected phytochemicals were evaluated using in silico ADMET prediction and molecular docking analyses. Acute oral toxicity was assessed in Wistar rats using Lorke’s method. Pre-formulation studies were conducted prior to capsule formulation using the wet granulation technique. The granules were evaluated for micromeritic properties, and the capsules were subjected to pharmacopoeial quality tests including weight uniformity, disintegration, and dissolution. The estimated LD₅₀ of the extract was 3.808 mg/kg body weight, indicating relatively low acute toxicity. Dissolution testing showed more than 80% release within 20 min under the experimental conditions employed. These findings suggest that the developed capsule formulation provides a suitable pharmaceutical dosage form for the hexane fraction of M. oleifera, although further studies including stability testing, quantitative phytochemical standardization, and pharmacological evaluation are required.