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Nanochemistry in Vaccine Delivery: Lipid Nanoparticles, Polymers, and Hybrid Systems Chandipwisa, Courage; Shimilimo, Agness; Zenda, Tendai Pride; Banda, Harrison
Sciences of Pharmacy Volume 5 Issue 1
Publisher : ETFLIN Publishing House

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Abstract

Conventional vaccines face challenges in antigen stability, delivery efficiency, and scalability, particularly in low- and middle-income countries. Nanochemistry offers innovative approaches through lipid nanoparticles, polymeric carriers, and hybrid systems. This review evaluates these platforms using criteria such as physicochemical properties, immunological outcomes, translational feasibility, and One Health relevance. A narrative literature review was conducted across major databases between 2015 and 2025. Studies were screened by title and abstract, excluded if not directly relevant to vaccine delivery, and weighted according to design, with clinical trials prioritized over in vitro or modeling studies. Reference lists of key papers were also examined to ensure comprehensive coverage. Lipid nanoparticles supported mRNA delivery in licensed COVID-19 vaccines, achieving strong immune responses but with variability across populations and reported adverse events including myocarditis and anaphylaxis. Polymeric nanoparticles such as PLGA and chitosan enabled controlled antigen release, though cost-effectiveness remains constrained by manufacturing and scalability challenges. Hybrid lipid-polymer systems demonstrated enhanced stability and multi-antigen presentation, with current evidence largely limited to preclinical studies. One Health implications are defined as the potential of nanochemistry to contribute to zoonotic disease prevention, food safety, and cross-species vaccine design, requiring clearer frameworks for integration. In conclusion, nanochemistry-based vaccine platforms show promise for advancing immunization strategies, but unresolved issues in safety evaluation, regulatory harmonization, and equitable access highlight the need for cautious interpretation and further interdisciplinary collaboration.
Harnessing plant secondary metabolites for vaccine development in Africa: Current insights and future prospects Chandipwisa, Courage; Banda, Harrison; Shimilimo, Agness
Sciences of Phytochemistry Volume 5 Issue 1
Publisher : ETFLIN

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Abstract

Plant secondary metabolites are natural compounds with immunomodulatory and adjuvant properties that may complement conventional vaccines and support regionally relevant vaccine strategies in Africa. This structured narrative review analyzed English-language studies published between 2000 and 2025 from PubMed, Google Scholar, Elsevier, and EBSCOhost. Included publications comprised original research, systematic reviews, and clinical trials addressing mechanisms, formulation, safety, and clinical development. Evidence included in vitro studies, animal models, formulation research, and human investigations. Preclinical findings show that selected metabolites enhance antigen presentation, promote dendritic cell maturation, and strengthen humoral and cellular immune responses through modulation of key signaling pathways. Triterpenoid saponins from Quillaja saponaria have progressed into clinical adjuvant platforms, while polysaccharides from Moringa oleifera and flavonoids from Curcuma longa and Artemisia annua demonstrate immunostimulatory effects and improved antigen stability in preclinical models. Nanoencapsulation improves compound stability and delivery but lacks sufficient clinical validation. Clinical translation requires standardized phytochemical characterization, comprehensive safety evaluation, regulatory harmonization, validated manufacturing processes, and adequately powered clinical trials with defined immunological endpoints.
Leveraging Artificial Intelligence to Strengthen Vaccine and Drug Development Capacity in Low-resource African Settings Chandipwisa, Courage; Banda, Harrison; Chabala, Kapembwa; Zenda, Tendai Pride; Shimilimo, Agness
Sciences of Pharmacy Volume 5 Issue 2
Publisher : ETFLIN

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Abstract

Africa’s vaccine and drug research and development capacity remains limited by infrastructural gaps, fragmented data systems, and shortages of skilled personnel, constraining timely therapeutic discovery and clinical translation in low-resource settings. Artificial intelligence (AI) and machine learning offer potential solutions by enabling predictive modelling, accelerating compound screening, improving genomic surveillance, and supporting adaptive clinical trial design. This narrative review synthesizes studies and institutional reports published between 2015 and 2025 from major scientific databases to examine AI applications in vaccine and drug development relevant to African contexts. Thematic analysis identified key patterns related to infrastructure readiness, workforce capacity, and translational implementation, with findings validated through evidence triangulation and consensus review. Results show that AI platforms have supported infectious disease candidate identification, pandemic vaccine development, malaria drug resistance mapping, and predictive analytics for vaccine distribution. While accelerated outcomes were evident during public health emergencies, routine implementation remains constrained by resource availability. Major challenges include inadequate digital infrastructure, fragmented regulatory systems, and limited technical expertise despite ongoing capacity-building initiatives. The review proposes an integrated framework linking infrastructure, skills development, and ethical governance as critical factors for sustainable AI adoption in African biomedical research. Strengthening investment, fostering regional collaboration, and developing context-specific ethical frameworks are essential to ensure equitable access, enhance innovation capacity, and build resilient biomedical research ecosystems across Africa.