Citation
Du, Ping, et al. "Development and Validation of a Rapid and Sensitive UPLC-MS/MS Method for Determination of Total Docetaxel From a Lipid Microsphere Formulation in Human Plasma." Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, vol. 926, 2013, pp. 101-7.
Du P, Li N, Wang H, et al. Development and validation of a rapid and sensitive UPLC-MS/MS method for determination of total docetaxel from a lipid microsphere formulation in human plasma. J Chromatogr B Analyt Technol Biomed Life Sci. 2013;926:101-7.
Du, P., Li, N., Wang, H., Yang, S., Song, Y., Han, X., & Shi, Y. (2013). Development and validation of a rapid and sensitive UPLC-MS/MS method for determination of total docetaxel from a lipid microsphere formulation in human plasma. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 926, 101-7. https://doi.org/10.1016/j.jchromb.2013.02.006
Du P, et al. Development and Validation of a Rapid and Sensitive UPLC-MS/MS Method for Determination of Total Docetaxel From a Lipid Microsphere Formulation in Human Plasma. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 May 1;926:101-7. PubMed PMID: 23567294.
TY - JOUR
T1 - Development and validation of a rapid and sensitive UPLC-MS/MS method for determination of total docetaxel from a lipid microsphere formulation in human plasma.
AU - Du,Ping,
AU - Li,Ning,
AU - Wang,Hongyu,
AU - Yang,Sheng,
AU - Song,Yuanyuan,
AU - Han,Xiaohong,
AU - Shi,Yuankai,
Y1 - 2013/03/13/
PY - 2012/12/10/received
PY - 2013/01/29/revised
PY - 2013/02/05/accepted
PY - 2013/4/10/entrez
PY - 2013/4/10/pubmed
PY - 2013/8/30/medline
SP - 101
EP - 7
JF - Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
JO - J Chromatogr B Analyt Technol Biomed Life Sci
VL - 926
N2 - Docetaxel lipid microsphere (DT-LM), an intravenous lipid emulsion for docetaxel without Tween 80, has demonstrated significant advantage over other conventional docetaxel formulations with respect to keeping sustained release, reducing irritation or toxicity of drug, sterile for intravenous injection and presenting targeting. A rapid, sensitive and reproducible ultra high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for determination of total docetaxel from a lipid microsphere formulation in human plasma using paclitaxel as internal standard (IS) has been developed and validated. The analytes and IS were extracted from plasma by simple liquid-liquid extraction and separated on ACQUITY UPLC BEH C18 column at a flow rate of 0.3 ml/min using gradient elution mode. The total analytical time was only 2.5 min. Detection and quantitation were performed by electrospray ionization (ESI) in the positive ionization mode by multiple reaction monitoring (MRM) of the transitions at m/z 808.3→527.1 for docetaxel and 854.0→285.9 for IS. The assay was linear over the concentration range of 2-5000 ng/ml (r(2)>0.99) with the lower limit of quantification (LLOQ) of 2 ng/ml. The intra- and inter-day precision in terms of relative standard deviation (RSD%) was within 9% and accuracy in terms of relative error (RE%) was within 12%. The rapid, sensitive and reproducible UPLC-MS/MS method is now used to support clinical pharmacologic studies with DT-LM injection in patients with advanced cancer.
SN - 1873-376X
UR - https://www.unboundmedicine.com/medline/citation/23567294/Development_and_validation_of_a_rapid_and_sensitive_UPLC_MS/MS_method_for_determination_of_total_docetaxel_from_a_lipid_microsphere_formulation_in_human_plasma_
L2 - https://linkinghub.elsevier.com/retrieve/pii/S1570-0232(13)00091-3
DB - PRIME
DP - Unbound Medicine
ER -