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Pranlukast Hemihydrate
Known as:
N-(4-Oxo-2-(1H-tetrazol-5-yl)-4H-1-benzopyran-8-yl)-p-(4-phenylbutoxy)benzamide Hemihydrate
, SC-215745
National Institutes of Health
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2019
2019
A simple blending with α-glycosylated naringin produces enhanced solubility and absorption of pranlukast hemihydrate.
Hiromasa Uchiyama
,
Kazunori Kadota
,
A. Nakanishi
,
M. Tandia
,
Y. Tozuka
International journal of pharmaceutics
2019
Corpus ID: 195806160
2015
2015
Improving dissolution and oral bioavailability of pranlukast hemihydrate by particle surface modification with surfactants and homogenization
Eun-Sol Ha
,
I. Baek
,
Jin-Wook Yoo
,
Yunjin Jung
,
Min‐Soo Kim
Drug Design, Development and Therapy
2015
Corpus ID: 2608125
The present study was carried out to develop an oral formulation of pranlukast hemihydrate with improved dissolution and oral…
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2013
2013
Self-microemulsifying drug-delivery system for improved oral bioavailability of pranlukast hemihydrate: preparation and evaluation
Myoung-Ki Baek
,
Jong-Hwa Lee
,
Y. Cho
,
Hak-Hyung Kim
,
Gye-Won Lee
International Journal of Nanomedicine
2013
Corpus ID: 12418635
The purpose of the present investigation was to develop and evaluate a self-microemulsifying drug delivery system (SMEDDS) for…
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2011
2011
α-Glucosyl hesperidin induced an improvement in the bioavailability of pranlukast hemihydrate using high-pressure homogenization.
Hiromasa Uchiyama
,
Y. Tozuka
,
Fusatoshi Asamoto
,
H. Takeuchi
International journal of pharmaceutics
2011
Corpus ID: 30420448
2007
2007
Preparation of drug nanoparticle-containing microparticles using a 4-fluid nozzle spray drier for oral, pulmonary, and injection dosage forms.
T. Mizoe
,
T. Ozeki
,
H. Okada
Journal of Controlled Release
2007
Corpus ID: 23139471
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