Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

Determination of plasma topotecan and its metabolite N-desmethyl topotecan as both lactone and total form by reversed-phase liquid chromatography with fluorescence detection.

Authors:
Feng Bai Mark N Kirstein Suzan K Hanna Lisa C Iacono Brad Johnston Clinton F Stewart

J Chromatogr B Analyt Technol Biomed Life Sci 2003 Feb;784(2):225-32

Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, 332 N. Lauderdale, 38105, Memphis, TN, USA.

Topotecan (TPT) undergoes hepatic N-demethylation forming N-desmethyl topotecan (NDS). To evaluate the effect of drug-drug interactions on NDS disposition in children receiving TPT we developed and validated a sensitive and specific HPLC-fluorescence detection method for lactone and total (lactone plus carboxylate) TPT and NDS. Deproteinized plasma is vortexed, centrifuged, and the methanolic extract diluted with water for the lactone form of NDS and TPT or diluted with 1.5% phosphoric acid for NDS and TPT total. A 100 microL sample is injected onto a Varian ChromGuard RP column attached to an Agilent SB-C(18) reversed-phase analytical column held at 50 degrees C. The mobile phase (flow-rate, 0.8 mL/min) consists of methanol-aqueous buffer (27:73, v/v) (75 mM potassium phosphate and 0.2% triethylamine, pH 6.5). TPT and NDS were detected with excitation and emission wavelengths set at 376 and 530 nm, respectively. The standard curves for both forms of TPT ranged from 0.25 to 80 ng/mL, and for NDS ranged from 0.10 to 8.0 ng/mL. Within-day and between-day precision (% RSD) was

Download full-text PDF

Source
http://dx.doi.org/10.1016/s1570-0232(02)00798-5DOI Listing
February 2003

Publication Analysis

Top Keywords

lactone total
8
nds tpt
8
n-desmethyl topotecan
8
tpt nds
8
tpt
7
nds
7
set 376
4
tpt diluted
4
form nds
4
lactone form
4
diluted 15%
4
determination plasma
4
15% phosphoric
4
tpt total
4
total 100
4
acid nds
4
phosphoric acid
4
wavelengths set
4
water lactone
4
diluted water
4

Keyword Occurance

Similar Publications

Tailored Synthesis of Skeletally Diverse Stemona Alkaloids through Chemoselective Dyotropic Rearrangements of β-Lactones.

Authors:
Yefeng Tang Zhen Guo Ruiyang Bao Yuanhe Li Yunshan Li Jingyang Zhang

Angew Chem Int Ed Engl 2021 Apr 13. Epub 2021 Apr 13.

Tsinghua University, Department of Chemistry, CHINA.

Collective synthesis of skeletally diverse Stemona alkaloids has been achieved, featuring tailored dyotropic rearrangements of b -lactones as key elements. Specifically, three typical 5/7/5 tricyclic skeletons associated with stemoamide, tuberostemospiroline and parvistemonine were first accessed through chemoselective alkyl-, hydrogen-, and aryl-migration dyotropic rearrangements of b -lactones, respectively. With rational manipulations of substrate structures and reaction conditions, these dyotropic rearrangements proceeded with excellent efficiency, good chemoselectivity and high stereospecificity. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Components identification and isomers differentiation in pigeon pea (Cajanus cajan L.) leaves by LC-MS.

Authors:
Zili Guo Peixi Zhu Xiaoai He Tianhe Yan Xianrui Liang

J Sep Sci 2021 Apr 8. Epub 2021 Apr 8.

Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, 310014, China.

A valid and reliable method based on ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry using electrospray ionization was established to identify chemical constituents in the ethanol extract of pigeon pea leaves. A total of 58 compounds were detected both in positive and negative modes. Among them, 42 compounds including 16 flavones, 1 flavonol, 5 flavanones, 9 isoflavones, 1 coumarin, 1 lactone, 6 stilbenes, 2 chalcones and 1 other compound were unambiguously identified or tentatively assigned in view of the retention time, the molecular formula as well as the fragmentation patterns. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Inhibition of Inducible Nitric Oxide Synthase (iNOS) by Andrographolide and Evaluation of Its Antiproliferative and Proapoptotic Effects on Cervical Cancer.

Authors:
Akbar Pasha Divya Vishambhar Kumbhakar Ravinder Doneti Kiran Kumar Gangappa Dharmapuri Pavan Kumar Poleboyina Heena S K Preethi Basavaraju Deepthi Pasumarthi Annapurna S D Pavani Soujanya I Arnold Emeson Vijayalaxmi Bodiga Smita C Pawar

Oxid Med Cell Longev 2021 16;2021:6692628. Epub 2021 Mar 16.

Department of Genetics & Biotechnology, University College of Science, Osmania University, Hyderabad, 500 007 Telangana, India.

This work is aimed at investigating the expression levels of inducible nitric oxide synthase (iNOS) in cervical cancer and identifying a potential iNOS inhibitor. The data mining studies performed advocated iNOS to be a promising biomarker for cancer prognosis, as it is highly overexpressed in several malignant cancers. The elevated iNOS was found to be associated with poor survival and increased tumor aggressiveness in cervical cancer. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones.

Authors:
Joonseong Hur Jaebong Jang Jaehoon Sim

Int J Mol Sci 2021 Mar 9;22(5). Epub 2021 Mar 9.

College of Pharmacy, Chungnam National University, Daejeon 34134, Korea.

-Butyrolactone, a five-membered lactone moiety, is one of the privileged structures of diverse natural products and biologically active small molecules. Because of their broad spectrum of biological and pharmacological activities, synthetic methods for -butyrolactones have received significant attention from synthetic and medicinal chemists for decades. Recently, new developments and improvements in traditional methods have been reported by considering synthetic efficiency, feasibility, and green chemistry. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

From Plant to Patient: Thapsigargin, a Tool for Understanding Natural Product Chemistry, Total Syntheses, Biosynthesis, Taxonomy, ATPases, Cell Death, and Drug Development.

Authors:
Søren Brøgger Christensen Henrik Toft Simonsen Nikolai Engedal Poul Nissen Jesper Vuust Møller Samuel R Denmeade John T Isaacs

Prog Chem Org Nat Prod 2021 ;115:59-114

Department of Oncology, Prostate Cancer Program, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Maryland, The Johns Hopkins University School of Medicine, Baltimore, The Bunting-Blaustein Cancer Research Building, 1650 Orleans Street, Baltimore, MD, 21231, USA.

Thapsigargin, the first representative of the hexaoxygenated guaianolides, was isolated 40 years ago in order to understand the skin-irritant principles of the resin of the umbelliferous plant Thapsia garganica. The pronounced cytotoxicity of thapsigargin is caused by highly selective inhibition of the intracellular sarco-endoplasmic Ca-ATPase (SERCA) situated on the membrane of the endo- or sarcoplasmic reticulum. Thapsigargin is selective to the SERCA pump and to a minor extent the secretory pathway Ca/Mn ATPase (SPCA) pump. Read More

View Article and Full-Text PDF
January 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap