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Article Abstract

Biocompatible nanocarriers were formulated by encapsulating medicinal extracts from (Red Bryony) and (Horned Poppy) using a nanophytosome approach. The nanophytosomes were prepared by employing a thin-film hydration technique. The SEM results showed a broad size distribution for both nanophytosomes, and the encapsulation efficiency was about 75-80% for both Red Bryony and Horned Poppy nanophytosomes, as confirmed through scanning electron microscopy (SEM) and dynamic light scattering (DLS). Zeta potential analysis indicated sufficient surface charges to maintain colloidal stability. Encapsulation improved the release characteristics of the extracts, exhibiting an initial burst release followed by sustained release, which is advantageous for enhancing bioavailability within a liquid environment. Fourier-transform infrared (FTIR) spectroscopy identified key functional groups, confirming the successful encapsulation of bioactive ingredients within the nanophytosomes. Cytotoxicity tests on fibroblast cell lines (HSF-PI 16) demonstrated the safety of these nanocarriers, indicating biocompatibility at concentrations up to 200 μg/mL. Stability tests over 30 days revealed minimal size fluctuations, further supporting the structural integrity of the formulations. Results suggest that the synthesized nanophytosomes could serve as effective and novel nanocarriers for herbal delivery, addressing the bioavailability limitations of herbal extracts and offering a promising approach for therapeutic applications in both traditional and alternative medicine. This is the first study to report nanophytosome-based delivery of Red Bryony and Horned Poppy extracts.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12193903PMC
http://dx.doi.org/10.3390/jfb16060194DOI Listing

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Article Synopsis
  • Oxidative stress and inflammation are key issues in immune-compromised diseases and cancer treatments, prompting a study on the immune-boosting effects of Bryonia alba (BA) in mice with induced immune deficiency.
  • The research involved treating BALB/c mice with various potencies of BA after cyclophosphamide administration, resulting in significant improvements in immune parameters like RBC and WBC levels, and increased expression of important immune cytokines.
  • Histopathology showed that BA-treated mice maintained healthy spleen structures compared to those damaged by cyclophosphamide, suggesting BA's potential as an effective immunostimulant during chemotherapy, but more studies are needed on its effects against immune-compromised infections.
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