Evidence map›Paper›PMID 38935286›Full record

ArticleApplied biochemistry and biotechnology2024

Antibacterial, Antifungal, and Cytotoxic Potential of PlumbaginLoaded pH-Responsive Vaginal Nanoformulations.

Tamil Mani Subi, Nandhakumar Selvasudha, Sivakumar Priyadharshini, Pradeep Kumar, Rakesh Singh, Hannah Rachel Vasanthi

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Article in Applied biochemistry and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Tamil Mani SubiNatural Products Research Laboratory, Department of Biotechnology, Pondicherry University, Puducherry, 605014, India.
Nandhakumar SelvasudhaNatural Products Research Laboratory, Department of Biotechnology, Pondicherry University, Puducherry, 605014, India.
Sivakumar PriyadharshiniNatural Products Research Laboratory, Department of Biotechnology, Pondicherry University, Puducherry, 605014, India.
Pradeep KumarDepartment of Microbiology, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, 605006, India.
Rakesh SinghDepartment of Microbiology, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, 605006, India.
Hannah Rachel VasanthiNatural Products Research Laboratory, Department of Biotechnology, Pondicherry University, Puducherry, 605014, India. hrvasanthi@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plumbagin is a naphthoquinone from the roots of the Plumbago species and exhibits anticancer activity. Translational usage of plumbagin in biomedical sciences is restricted due to its poor solubility and bioavailability. Therefore, pH-responsive plumbagin-loaded vaginal nanoformulations with polylactic acid (PLA)-chitosan polymeric coat were fabricated by inotropic gelation technique. Among the four (F1, F2, F3, F4) nanoformulations prepared, F3 exhibited good interaction of polymers with plumbagin as evidenced by FTIR, XRD, and thermal analysis. The positive zeta potential (48.4 ± 5.57 mV), optimal size (694 ± 65.76 nm), low PDI (0.157), and good encapsulation efficiency (77.8 ± 3.62%) of F3 were significant. The indirect method of drug loading (58.35 ± 5.00%) confirmed the drug content of about 495.44 ± 5.00 µg of plumbagin in 1 mg of F3. The drug loading pattern was confirmed by TEM analysis, and the spherical morphology of the nanocomposite was confirmed by SEM analysis. F3 formulation showed 46% and 25.2% of drug release in 24 h in simulated vaginal fluid at pH 4.5 and 7 respectively with sustained release and hydrolyses of lactic acid from PLA. Among all the nanoformulations evaluated, nanoformulation F3 with promising physicochemical properties showed good antifungal and antibacterial activity against various fungal and bacterial strains. F3 exhibited potent cytotoxicity with an IC50 of 3.6 ± 0.12 µg/ml for HeLa and an IC50 of 0.81 ± 0.01 µg/ml for SiHa cells. Altogether, the nanoformulation F3 exhibited potent antimicrobial activity against vaginal infections and cytotoxicity against cervical cancer cell lines.

Indexed as

Anti-Bacterial AgentsAntifungal AgentsNaphthoquinonesChitosanDrug CarriersFemaleHeLa CellsHumansHydrogen-Ion ConcentrationMicrobial Sensitivity TestsPolyestersVaginaAnti-Bacterial AgentsAntifungal AgentsChitosanDrug CarriersNaphthoquinonesplumbaginPolyesterspoly(lactide)Inotropic gelationNanoformulationspH-responsivePlumbaginVaginal

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.