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A UFLC-MS/MS method coupled with one-step protein precipitation for determination of docetaxel in rat plasma: comparative pharmacokinetic study of modified nanostructured lipid carrier.
J Pharm Biomed Anal. 2013 Sep; 83:202-8.JP

Abstract

A rapid, simple and sensitive ultra fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) method coupled with one-step protein precipitation procedure has been developed and validated for the pharmacokinetic study of docetaxel in rat plasma to investigate the influence of polyethylene glycol (PEG) molecular weights (chain length) using in the modified formulations. Separation was achieved on a Venusil MP C18 column (100 mm × 2.1 mm, 3.0 μm) with a mobile phase consisting of methanol-water, and the total running time was 3.5min. The standard curve was linear over the range of 5-5000 ng/mL, with lower limits of quantification (LLOQ) of 5 ng/mL. The method was shown to be reliable and reproducible with intra-day precision below 10.7%, inter-day precision below 11.2%, accuracy within ±5.2%, and mean extraction recovery of 84.6-90.2%. The validated method was successfully applied to the comparative pharmacokinetic study of docetaxel in rat plasma after intravenous administration of docetaxel-loaded nanostructured lipid carrier modified by copolymers consisting of series of PEG molecular weights (2000, 4000, 10,000 Da), respectively. The results indicated that PEG-4000 possessed a better and longer circulation effect, which made the modified formulation one of the promising suspensions for the delivery of docetaxel in cancer.

Authors+Show Affiliations

School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenhe District, Shenyang, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23764658

Citation

Zhao, Xu, et al. "A UFLC-MS/MS Method Coupled With One-step Protein Precipitation for Determination of Docetaxel in Rat Plasma: Comparative Pharmacokinetic Study of Modified Nanostructured Lipid Carrier." Journal of Pharmaceutical and Biomedical Analysis, vol. 83, 2013, pp. 202-8.
Zhao X, Bi K, Wang X, et al. A UFLC-MS/MS method coupled with one-step protein precipitation for determination of docetaxel in rat plasma: comparative pharmacokinetic study of modified nanostructured lipid carrier. J Pharm Biomed Anal. 2013;83:202-8.
Zhao, X., Bi, K., Wang, X., Xue, X., He, B., Cui, Y., Liu, Z., Wang, D., & Chen, X. (2013). A UFLC-MS/MS method coupled with one-step protein precipitation for determination of docetaxel in rat plasma: comparative pharmacokinetic study of modified nanostructured lipid carrier. Journal of Pharmaceutical and Biomedical Analysis, 83, 202-8. https://doi.org/10.1016/j.jpba.2013.05.025
Zhao X, et al. A UFLC-MS/MS Method Coupled With One-step Protein Precipitation for Determination of Docetaxel in Rat Plasma: Comparative Pharmacokinetic Study of Modified Nanostructured Lipid Carrier. J Pharm Biomed Anal. 2013;83:202-8. PubMed PMID: 23764658.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A UFLC-MS/MS method coupled with one-step protein precipitation for determination of docetaxel in rat plasma: comparative pharmacokinetic study of modified nanostructured lipid carrier. AU - Zhao,Xu, AU - Bi,Kaishun, AU - Wang,Xiaofan, AU - Xue,Xiao, AU - He,Bosai, AU - Cui,Yan, AU - Liu,Zhenzhen, AU - Wang,Dongkai, AU - Chen,Xiaohui, Y1 - 2013/05/25/ PY - 2013/02/14/received PY - 2013/05/15/revised PY - 2013/05/17/accepted PY - 2013/6/15/entrez PY - 2013/6/15/pubmed PY - 2014/3/25/medline SP - 202 EP - 8 JF - Journal of pharmaceutical and biomedical analysis JO - J Pharm Biomed Anal VL - 83 N2 - A rapid, simple and sensitive ultra fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) method coupled with one-step protein precipitation procedure has been developed and validated for the pharmacokinetic study of docetaxel in rat plasma to investigate the influence of polyethylene glycol (PEG) molecular weights (chain length) using in the modified formulations. Separation was achieved on a Venusil MP C18 column (100 mm × 2.1 mm, 3.0 μm) with a mobile phase consisting of methanol-water, and the total running time was 3.5min. The standard curve was linear over the range of 5-5000 ng/mL, with lower limits of quantification (LLOQ) of 5 ng/mL. The method was shown to be reliable and reproducible with intra-day precision below 10.7%, inter-day precision below 11.2%, accuracy within ±5.2%, and mean extraction recovery of 84.6-90.2%. The validated method was successfully applied to the comparative pharmacokinetic study of docetaxel in rat plasma after intravenous administration of docetaxel-loaded nanostructured lipid carrier modified by copolymers consisting of series of PEG molecular weights (2000, 4000, 10,000 Da), respectively. The results indicated that PEG-4000 possessed a better and longer circulation effect, which made the modified formulation one of the promising suspensions for the delivery of docetaxel in cancer. SN - 1873-264X UR - https://www.unboundmedicine.com/medline/citation/23764658/A_UFLC_MS/MS_method_coupled_with_one_step_protein_precipitation_for_determination_of_docetaxel_in_rat_plasma:_comparative_pharmacokinetic_study_of_modified_nanostructured_lipid_carrier_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0731-7085(13)00226-4 DB - PRIME DP - Unbound Medicine ER -