Aim & Objective: This study evaluates the potential of combining paclitaxel (PTX) and bortezomib (BTZ) for breast cancer therapy.Materials & Methods: The nanoformulation was optimized via Box-Behnken Design (BBD), with method validation adhering to US-FDA guidelines.Results: Multiple reaction monitoring transitions for PTX, BTZ and internal standard were m/z 855.80â286.60, 366.80â226.00 and 179.80â110.00, respectively. Elution done on C18 Luna column with 0.1% FA in MeOH:10 mM ammonium acetate. The size of nanoformulation was 133.9 ± 1.97 nm, PDI 0.19 ± 0.01 and zeta potential -19.20 ± 1.36 mV. Pharmacokinetics showed higher C(max) for PTX-BTZ-NE (313.75 ± 10.71 ng/ml PTX, 11.92 ± 0.53 ng/ml BTZ) versus free PTX-BTZ (104 ± 13.06 ng/ml PTX, 1.9 ± 0.08 ng/ml BTZ).Conclusion: Future findings will contribute to the treatment of breast cancer using PTX and BTZ.
Simultaneous estimation of paclitaxel and bortezomib via LC-MS/MS: pharmaceutical and pharmacokinetic applications.
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作者:Yadav Pavan K, Verma Saurabh, Chauhan Divya, Yadav Pooja, Tiwari Amrendra K, Saklani Ravi, Gupta Deepak, Rana Rafquat, Shah Aarti Abhishek, Verma Sonia, Naresh Kothuri, Gayen Jiaur R, Chourasia Manish K
| 期刊: | Nanomedicine | 影响因子: | 3.900 |
| 时间: | 2024 | 起止号: | 2024;19(24):1995-2010 |
| doi: | 10.1080/17435889.2024.2382668 | ||
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