CD44 tagged hyaluronic acid - chitosan liposome carrier for the delivery of berberine and doxorubicin into lung cancer cells

被引:23
|
作者
Maheswari, Ramakrishna Thilagar Uma [1 ]
Ajithkumar, Velmurugan [2 ]
Varalakshmi, Perumal [2 ]
Rajan, Mariappan [1 ]
机构
[1] Madurai Kamaraj Univ, Sch Chem, Dept Nat Prod Chem, Biomat Med Chem Lab, Madurai 625021, Tamil Nadu, India
[2] Madurai Kamaraj Univ, Sch Biotechnol, Dept Mol Microbiol, Madurai 625021, Tamil Nadu, India
关键词
Berberine; Hyaluronic acid; Liposome; Multilayer carrier; Targeted drug delivery; PHYSICOCHEMICAL CHARACTERIZATION; THERAPEUTIC-EFFICACY; DRUG-DELIVERY; NANOPARTICLES; APOPTOSIS; STATE; FORM;
D O I
10.1016/j.ijbiomac.2023.126599
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liposomes are unique biomolecular, capable of loading both hydrophilic and hydrophobic molecules and delivered into the biological system. Liposomes (L) coated with hyaluronic acid (HA) and chitosan (CS) carrier system was fabricated. Berberine (BER) and doxorubicin (DOX) were encapsulated to enhance drug proliferation and therapeutic effect in lung cancer cells. The FTIR, XRD, SEM, and TEM techniques were carried out for functional group identification, crystallinity, and surface morphology analysis, respectively. In-vitro drug release confirms the sustained release of BER and DOX in various physiological environments. HA-CS@BER&DOX-L has good penetration ability and higher cytotoxicity effect in the A549 cells, and the IC50 value of HACS@BER&DOX-L is 89.19 mu g/300 mu L. The pure liposome showed a negligible cytotoxicity effect, and the HACS@BER&DOX-L could efficiently induce the apoptosis of A549 cells. The cellular uptake analysis of the HACS@BER&DOX-L effectively targeted and entered the A549 cells and clearly observed C. elegans images. Hence, the proposed system will be a potential treatment methodology to enhance the cytotoxicity of the A549 cancer cells and be useful to future drug administration methodology development.
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页数:12
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