Zobrazeno 1 - 10
of 32
pro vyhledávání: '"D M Oh"'
Publikováno v:
The Review of scientific instruments. 91(1)
We have designed, constructed, and tested an electrical vacuum feedthrough that can carry a large number of microwave signal lines, has high vacuum compatibility, and is highly customizable. We found that it had a leak rate of approximately 10-7 Pa L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0e5f9774a68ed3bb4956337439a17e5
https://pubmed.ncbi.nlm.nih.gov/32012540
https://pubmed.ncbi.nlm.nih.gov/32012540
Publikováno v:
Acta Horticulturae. :71-72
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fc16d4bfdabd9b7d1cb08c3f19547eb
https://doi.org/10.17660/actahortic.2015.1093.6
https://doi.org/10.17660/actahortic.2015.1093.6
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 299(2)
The proton-coupled oligopeptide transporter (PEPT1) has been shown to mediate mucosal cell transport of di- and tripeptide, and some peptidomimetic drugs. In this study, we determined the correlation between PEPT1 protein expression and the permeabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bdea05418dd1243b191c66f1743c46d2
https://pubmed.ncbi.nlm.nih.gov/11602669
https://pubmed.ncbi.nlm.nih.gov/11602669
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 238(8)
Background: Our studies had indicated that optic disc vasculitis (ODV) is a distinct clinical entity. We investigated the presentation and clinical characteristics of ODV and determined the efficacy of systemic corticosteroids in its management. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5e445604b0e0133249e5c7a4de5110d
https://pubmed.ncbi.nlm.nih.gov/11011684
https://pubmed.ncbi.nlm.nih.gov/11011684
Autor:
D M, Oh, G L, Amidon
Publikováno v:
Pharmaceutical biotechnology. 12
Pharmaceutical scientists increasingly utilize transporters for drug delivery and targeting. The biological barriers to drug delivery can basically be divided into epithelial, endothelial, elimination, and target cell barriers. Membrane transporters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2e0cc9e8d297e7314fc04df1f5790695
https://pubmed.ncbi.nlm.nih.gov/10742970
https://pubmed.ncbi.nlm.nih.gov/10742970
Publikováno v:
Pharmaceutical biotechnology. 12
A wide variety of transporters are found in the intestine, and are involved in the membrane transport of daily nutrients as well as drugs. These intestinal transporters are located in the brush border membrane as well as basolateral membrane. Each tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e72ecc379d02faf50a325e3cc3672552
https://pubmed.ncbi.nlm.nih.gov/10742972
https://pubmed.ncbi.nlm.nih.gov/10742972
Publikováno v:
Journal of pharmaceutical sciences. 89(2)
This study reports the results of the combined effect of pH and surfactant on the dissolution of piroxicam (PX), an ionizable water-insoluble drug in physiological pH. The intrinsic dissolution rate (J(total)) of PX was measured in the pH range from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9090171fb1b9b3525175f24708f13ed
https://pubmed.ncbi.nlm.nih.gov/10688756
https://pubmed.ncbi.nlm.nih.gov/10688756
Autor:
N, Surendran, K M, Covitz, H, Han, W, Sadee, D M, Oh, G L, Amidon, R M, Williamson, C F, Bigge, B H, Stewart
Publikováno v:
Pharmaceutical research. 16(3)
The objective of this research was to investigate the substrate specificity of large neutral amino acid carrier (LNAA) and di/tripeptide (hPEPT1) transporters with respect to PD 158473, an NMDA antagonist.Cellular uptake studies were carried out usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c93cd38f076c1044ff81cc9d89926e65
https://pubmed.ncbi.nlm.nih.gov/10213369
https://pubmed.ncbi.nlm.nih.gov/10213369
Publikováno v:
Pharmaceutical research. 15(9)
This study characterized the cellular uptake mechanism and hydrolysis of the amino acid ester prodrugs of nucleoside antiviral drugs in the transiently transfected Caco-2 cells overexpressing a human intestinal peptide transporter, hPEPT1 (Caco-2/hPE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56bd75115d8343684195d21ffdc3e6a9
https://pubmed.ncbi.nlm.nih.gov/9755889
https://pubmed.ncbi.nlm.nih.gov/9755889
Autor:
H, Han, R L, de Vrueh, J K, Rhie, K M, Covitz, P L, Smith, C P, Lee, D M, Oh, W, Sadée, G L, Amidon
Publikováno v:
Pharmaceutical research. 15(8)
General use of nucleoside analogues in the treatment of viral infections and cancer is often limited by poor oral absorption. Valacyclovir, a water soluble amino acid ester prodrug of acyclovir has been reported to increase the oral bioavailability o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::383e706e0f29f968047c7fa572b747b2
https://pubmed.ncbi.nlm.nih.gov/9706043
https://pubmed.ncbi.nlm.nih.gov/9706043