Ratiometric codelivery of Paclitaxel and Baicalein loaded nanoemulsion for enhancement of breast cancer treatment

[Display omitted] •Codelivery of Paclitaxel (PTX) and Baicalein (BCLN) exhibited a good synergistic effect.•PTX-BCLN loaded nanoemulsion showed improved in vitro release compared to the free drug.•Enhanced antitumor efficacy was found with PTX-BCLN nanoemulsion compared to other formulation treatmen...

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Veröffentlicht in:International journal of pharmaceutics 2023-08, Vol.643, p.123209-123209, Article 123209
Hauptverfasser: Yadav, Pavan K., Saklani, Ravi, Tiwari, Amrendra K., Verma, Saurabh, Chauhan, Divya, Yadav, Pooja, Rana, Rafquat, Kalleti, Navodayam, Gayen, Jiaur R., Wahajuddin, Rath, Srikanta K., Mugale, Madhav N., Mitra, Kalyan, Chourasia, Manish K.
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Sprache:eng
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Zusammenfassung:[Display omitted] •Codelivery of Paclitaxel (PTX) and Baicalein (BCLN) exhibited a good synergistic effect.•PTX-BCLN loaded nanoemulsion showed improved in vitro release compared to the free drug.•Enhanced antitumor efficacy was found with PTX-BCLN nanoemulsion compared to other formulation treatments.•Nanoemulsion maintained both drugs synergistic molar weight ratio at the tumor site.•Nanoformulation showed better biosafety and animal survival in comparison to free drug treatment. The most prevalent clinical option for treating cancer is combination chemotherapy. In combination therapy, assessment and optimization for obtaining a synergistic ratio could be obtained by various preclinical setups. Currently, in vitro optimization is used to get synergistic cytotoxicity while constructing combinations. Herein, we co-encapsulated Paclitaxel (PTX) and Baicalein (BCLN) with TPP-TPGS1000 containing nanoemulsion (TPP-TPGS1000-PTX-BCLN-NE) for breast cancer treatment. The assessment of cytotoxicity of PTX and BCLN at different molar weight ratios provided an optimized synergistic ratio (1:5). Quality by Design (QbD) approach was later applied for the optimization as well as characterization of nanoformulation for its droplet size, zeta potential and drug content. TPP-TPGS1000-PTX-BCLN-NE significantly enhanced cellular ROS, cell cycle arrest, and depolarization of mitochondrial membrane potential in the 4T1 breast cancer cell line compared to other treatments. In the syngeneic 4T1 BALB/c tumor model, TPP-TPGS1000-PTX-BCLN-NE outperformed other nanoformulation treatments. The pharmacokinetic, biodistribution and live imaging studies pivoted TPP-TPGS1000-PTX-BCLN-NE enhanced bioavailability and PTX accumulation at tumor site. Later, histology studies confirmed nanoemulsion non-toxicity, expressing new opportunities and potential to treat breast cancer. These results suggested that current nanoformulation can be a potential therapeutic approach to effectively address breast cancer therapy.
ISSN:0378-5173
1873-3476
DOI:10.1016/j.ijpharm.2023.123209