Zobrazeno 1 - 10
of 23
pro vyhledávání: '"D. A. Boulton"'
Publikováno v:
Annals of Pharmacotherapy. 29:987-990
Objective: To assess the stability, dosage uniformity, and clinical acceptability of hydrocortisone oral suspensions prepared from tablets and powder. Design: Hydrocortisone 2.5 mg/mL oral suspensions were stored in the dark for 91 days at 5, 25, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50747932c0cac0a68eac1aba35acf18f
https://doi.org/10.1177/106002809502901005
https://doi.org/10.1177/106002809502901005
Publikováno v:
Journal of clinical pharmacy and therapeutics. 37(5)
The antipsychotic, aripiprazole, plus lithium or valproate demonstrates rapid and significant improvement in manic symptoms that is sustained over the long term. A previous report showed that therapeutic doses of either lithium or valproate had no cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9ecdee8293dddf39b8ec38fedfb011a
https://pubmed.ncbi.nlm.nih.gov/22943745
https://pubmed.ncbi.nlm.nih.gov/22943745
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8b927ab7716d6040d5b4e6d62b778e2
https://doi.org/10.1111/j.1365-2710.2012.1331.x
https://doi.org/10.1111/j.1365-2710.2012.1331.x
Autor:
D. I. Boulton, A. C. Adams
Publikováno v:
5th IET International Conference on System Safety 2010.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcdd5229fd37c35fa5691df571a551c6
https://doi.org/10.1049/cp.2010.0842
https://doi.org/10.1049/cp.2010.0842
Autor:
Jian Wang, Donna M. Barten, J Lubinski, R Krishna, J J Anderson, K M Felsenstein, S B Hansel, A Thakur, D W Boulton, K S Santone, Ming Yao, Ming Zheng, J M Pursley, Oliver P. Flint
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 39(7)
BMS-299897 is a gamma-secretase inhibitor that was effective in reducing amyloid beta-peptide (A beta) in transgenic mice and guinea pigs. Therefore, pharmacokinetic and drug metabolism studies were conducted in animals to support its clinical develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0298721585ee00fb36703598090556
https://pubmed.ncbi.nlm.nih.gov/19480557
https://pubmed.ncbi.nlm.nih.gov/19480557
Autor:
D W, Boulton, C L, Devane
Publikováno v:
Chirality. 12(9)
Methadone enantiomers and EDDP, the main metabolite of methadone, were separated (R(s) = 2.0 for methadone enantiomers) following liquid-liquid extraction from human serum and urine followed by reverse-phase high-performance liquid chromatography on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::16583b1ff446ec6ea60a4ed9224bb9cf
https://pubmed.ncbi.nlm.nih.gov/10984743
https://pubmed.ncbi.nlm.nih.gov/10984743
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 28(6)
Ethylphenidate was recently reported as a novel drug metabolite in two overdose fatalities where there was evidence of methylphenidate and ethanol coingestion. This study explores the pharmacokinetics of ethylphenidate relative to methylphenidate and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70b93e9fbff94228fc29880386143af6
https://pubmed.ncbi.nlm.nih.gov/10820132
https://pubmed.ncbi.nlm.nih.gov/10820132
Publikováno v:
British journal of clinical pharmacology. 47(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c8433c9931f9ba9219a127439c06606
https://pubmed.ncbi.nlm.nih.gov/10400466
https://pubmed.ncbi.nlm.nih.gov/10400466
Autor:
D. W. Boulton, J. P. Fawcett
Publikováno v:
European journal of clinical pharmacology. 53(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59ac78992c2257a02b091ead55784776
https://pubmed.ncbi.nlm.nih.gov/9516040
https://pubmed.ncbi.nlm.nih.gov/9516040
Publikováno v:
American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists. 53(10)
The stability of levothyroxine sodium in oral liquid dosage forms compounded from commercially available tablets was studied. Levothyroxine sodium oral liquids (25 micrograms/mL) were prepared from tablets and from powder with and without methylparab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30725373c0c5a415370c3d487d8b1dc9
https://pubmed.ncbi.nlm.nih.gov/8734676
https://pubmed.ncbi.nlm.nih.gov/8734676