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			<edb:english>Encapsulation of an antivasospastic drug, fasudil, into loposomes, and in vitro stability of the fasdil-loaded liposomes</edb:english>
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			<edb:english>Int. J. Pharm</edb:english>
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			<edb:english>10.1016/S0378-5173(01)00896-1</edb:english>
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			<edb:english>read0170980/misc/12964423</edb:english>
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			<edb:english>Effect of Cationic Liposomes in an in Vitro Transcription and Translation System</edb:english>
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			<edb:english>Biol. Pharm. Bull</edb:english>
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			<edb:english>20020000</edb:english>
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			<edb:english>10.1248/bpb.25.529</edb:english>
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			<edb:english>Quantitative Analysis of Correlation between Number of Nuclear Plasmids and Gene Expression Activity after Transfection with Cationic Liposomes</edb:english>
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			<edb:english>Pharmaceutical Research</edb:english>
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			<edb:english>20020000</edb:english>
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			<edb:english>10.1023/A:1015162722295</edb:english>
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			<edb:english>HEPC-based loposomes trigger cytokine release from periferal blood cells : Effects of loposomal size, does and lipid composition</edb:english>
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			<edb:english>International Journal of Pharmaceutics</edb:english>
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			<edb:english>10.1016/S0378-5173(02)00026-1</edb:english>
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			<edb:english>read0170980/misc/12964420</edb:english>
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			<edb:english>Masahito Komuro</edb:english>
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			<edb:english>Yasuro Kawaguchi</edb:english>
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			<edb:english>Kazuho Okudaira</edb:english>
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			<edb:english>Masahiro Hayashi</edb:english>
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			<edb:english>Hiroshi Kiwada</edb:english>
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			<edb:english>Ryotaro Azuma</edb:english>
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			<edb:english>Comparative Analysis of In Vitro and In Vivo Pharmacokinetic Parameters Related to Individual Variability of GTS-21 in Canine</edb:english>
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			<edb:english>Drug Metabolism and Pharmacokinetics</edb:english>
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			<edb:english>The complement system enhances the clearance of phosphatidylserine (PS)-liposomes in rat and guinea pig</edb:english>
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			<edb:english>International Journal of Pharmaceutics</edb:english>
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			<edb:english>Soecies Difference in Correlation between in Vivo/in Vitro Lioposome-Complement Interactions</edb:english>
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			<edb:english>Efficacy of Intrathecal Liposomal Fasudil for Experinental Cerebral Vasospasm afte Subarachnoid Hemorrhage</edb:english>
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			<edb:english>Neurosugery</edb:english>
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			<edb:english>Intracellular control of gene trafficking using liposomes as drug carriers</edb:english>
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			<edb:english>Eur. J. Pharm. Sci.</edb:english>
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			<edb:english>Effect of cholesterol content in activation of the classical versus the alternative pathway of rat complement system induced by hydrogenated egg phosphatidycholine-based liposomes</edb:english>
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			<edb:english>Int. J. Pharm</edb:english>
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			<edb:english>10.1016/S0378-5173(01)00737-2</edb:english>
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			<edb:english>Intracellular control of macromolecules by use of liposomes as drug carriers</edb:english>
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			<edb:english>J. Biol. Macromol.</edb:english>
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			<edb:english>First-pass of GTS-21 on cacine gut wall and liver determined by portal-systemic concentration difference</edb:english>
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			<edb:english>Interactions of Liposomes with Cells In Vitro and In Vivo: Opsonins and Receptors</edb:english>
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			<edb:english>Current Drug Metabolism</edb:english>
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			<edb:english>Quantitative studies on the nuclear transport of plasmid DNA and gene expression employing nonviarl vectors</edb:english>
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			<edb:english>Advanced Drug Delivery Reviews</edb:english>
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			<edb:japanese>有効性の向上とバイオアベイラビリティー</edb:japanese>
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			<edb:english>Biodistribution of liposomes and C3 fragments associated with liposomes: evaluation of their reltionship</edb:english>
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			<edb:english>Int. J. Pharm</edb:english>
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			<edb:english>10.1016/S0378-5173(00)00511-1</edb:english>
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			<edb:japanese>血中滞留性リポソームによる抗癌剤の処方設計における最適化</edb:japanese>
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			<edb:english>Hideyoshi Harashima</edb:english>
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			<edb:english>Studies on the mechanism of uptake of liposomes using an isolated perfused liver system</edb:english>
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			<edb:english>Informa Healthcare</edb:english>
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			<edb:english>Journal of Liposome Research</edb:english>
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			<edb:english>10.3109/08982109609037202</edb:english>
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			<edb:english>Size-dependent release of carboxyfluorescein from cetylmannoside-modifide liposomes in human plasma</edb:english>
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			<edb:english>Is control of distribution of liposomes between tumors and bone marrow possible ?</edb:english>
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			<edb:japanese>リポソームによるDDS</edb:japanese>
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			<edb:english>Effect of vesicle size on in vivo release of daunorubicin from hydrogenated egg phosphatidylcholine-based liposomes into blood circulation</edb:english>
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			<edb:english>Hirotami MATSUO</edb:english>
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			<edb:english>Chikamasa YAMASHITA</edb:english>
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			<edb:japanese>ヒドラジン遊離薬物からのフリーラジカルの生成とアスコルビン酸の効果</edb:japanese>
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			<edb:english>Kinetic analysis of tissue distribution of doxorubicin incorporated in liposomes in rats (]G0001[)</edb:english>
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		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964391</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:japanese>イソニアジドのフリーラジカル中間代謝物に及ぼすアスコルビン酸の影響</edb:japanese>
		</edb:article.title>
		<edb:article.magazine>
			<edb:japanese>薬学雑誌</edb:japanese>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>111</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>10</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>600 605</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1248/yakushi1947.111.10_600</edb:english>
		</edb:article.doi>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964390</edb:english>
		</edb:article.researchmap>
		<edb:article.author>
			<edb:english>KUME Yoshihiro</edb:english>
			<edb:japanese>久米義博</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>YAMANE Chizu</edb:english>
			<edb:japanese>山根千鶴</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>HARASHIMA Hideyoshi</edb:english>
			<edb:japanese>原島秀吉</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>KIWADA Hiroshi</edb:english>
			<edb:japanese>際田弘志</edb:japanese>
		</edb:article.author>
		<edb:article.title>
			<edb:english>Quantitative analysis of the stability of liposomes in blood in vivo.</edb:english>
			<edb:japanese>In vivo実験系における血中でのリポソームの安定性の定量的評価法</edb:japanese>
		</edb:article.title>
		<edb:article.summary>
			<edb:english>To evaluate the stability of liposomes &lt;I&gt;in vivo&lt;/I&gt; is an important issue in the kinetic analysis of liposomes disposition, because the leakage of liposomal marker occurs &lt;I&gt;in vivo&lt;/I&gt; blood circulation and this leads to incorrect measurement of blood concentration of intact liposomes. In this study, we developed novel quantitative method for the evaluation of the stability of liposomes in blood circulation based on the clearance concept for liposomal degradation. Inulin was used as an aqueous marker of liposomes, because it is impermeable through a biological membrane and is rapidly excreted solely by glomerular filtration. We have further examined the effect of time delay of inulin during the passage of ureter to bladder on the estimation of the free fraction, using deconvolution method. The results showed that this delay was small enough to be neglected in the practical calculation. The degradation clearance of the liposomes in &lt;I&gt;in vivo&lt;/I&gt; study was calculated as [f/(1-f)·GFR], where f, GFR are the fraction of free concentration of inulin in blood, and glomerular filtrationr ate. On the other hand, the degradation clearance of the liposomes in &lt;I&gt;in vitro&lt;/I&gt; study was calculated as(dose/AUC), where AUC was the area under the time course of the concentration of intact liposomes from t=0 to infinite. The &lt;I&gt;in vivo&lt;/I&gt; clearance was 0.0214m&lt;I&gt;l&lt;/I&gt;/min, while &lt;I&gt;in vitro&lt;/I&gt; one was 0.00103m&lt;I&gt;l&lt;/I&gt;/min. There was about 20-fold difference. It shows that the &lt;I&gt;in vitro&lt;/I&gt; data is not appropriate for the ananlysis of &lt;I&gt;in vivo&lt;/I&gt; data. This method of evaluation of liposome stability in vivo is simple and useful in the pharmacokinetic study of liposomes.</edb:english>
		</edb:article.summary>
		<edb:article.publisher>
			<edb:english>The Japanese Society for the Study of Xenobiotics</edb:english>
		</edb:article.publisher>
		<edb:article.magazine>
			<edb:english>Drug Metabolism and Pharmacokinetics</edb:english>
			<edb:japanese>薬物動態</edb:japanese>
			<edb:article.magazine.issn>
				<edb:english>0916-1139</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>6</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>2</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>201 208</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.2133/dmpk.6.201</edb:english>
		</edb:article.doi>
		<edb:article.language mapto="60002"/>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964389</edb:english>
		</edb:article.researchmap>
		<edb:article.author>
			<edb:english>Yamashita Chikamasa</edb:english>
			<edb:japanese>山下 親正</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Sone Saburo</edb:english>
			<edb:japanese>曽根 三郎</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Ogura Takeshi</edb:english>
			<edb:japanese>小倉 剛</edb:japanese>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Kiwada Hiroshi</edb:english>
			<edb:japanese>際田 弘志</edb:japanese>
		</edb:article.author>
		<edb:article.title>
			<edb:english>Enhancing effect of monocytes survival by recombinant human macrophage colony-stimulating factor encapsulated in cetylmannoside-modified liposomes.</edb:english>
			<edb:japanese>マクロファージコロニー刺激因子含有マンノース修飾リポソームによるヒト単球の生存率増強効果</edb:japanese>
		</edb:article.title>
		<edb:article.summary>
			<edb:english>The present study was undertaken to examine potential value of cetlymannosides-modified multilamellar liposomes(Man-MLV)as vehicle of recombinant human macrophage colony-stimulating factor (M-CSF) to human blood monocytes. Man-MLV was taken effectively by monocytes as compared with liposomes without cetylmannoside (PC-MLV). Addition of D-mannose(50 mM) inhibited about 50% of uptake of Man-MLV by monocytes, but not significantly uptake of PC-MLV by monocytes. These results suggest that mannose redisues of Man-MLV contributes to uptake of Man-MLV by monocytes. We examined effect of encapsulation of M-CSF in Man-MLV on survival prolongation of monocytes. Blood monocytes that had been incubated for 7 days in medium with M-CSF encapsulated in Man-MLV were effective in prolongation of monocytes survival. This enhancing effect by M-CSF encapsulated in Man-MLV showed about 5-10 times higher than that in PC-MLV, in spite of the uptake of Man-MLV by monocytes was only about 2-fold different from that of PC-MLV. It was suspected that this effect contributes to not only effective uptake by monocytes, but also the difference of intracellular disposition of liposomes in monocytes. These results suggest that Man-MLV may be effective carrier vehicle in &lt;i&gt;in vivo&lt;/i&gt; delivery of M-CSF to human blood monocytes.</edb:english>
		</edb:article.summary>
		<edb:article.publisher>
			<edb:english>THE JAPAN SOCIETY OF DRUG DELIVERY SYSTEM</edb:english>
			<edb:japanese>日本DDS学会</edb:japanese>
		</edb:article.publisher>
		<edb:article.magazine>
			<edb:english>Drug Delivery System</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0913-5006</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>6</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>1</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>19 24</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.2745/dds.6.19</edb:english>
		</edb:article.doi>
		<edb:article.language mapto="60002"/>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964345</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:english>Targeting to mononuclear phagocyte system by cetylmannoside-modified liposomes</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>J. Phamacobio-Dyn. ,</edb:english>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>14</edb:english>
		</edb:article.volume>
		<edb:article.page>
			<edb:english>S-72 null</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964338</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:english>Saturable, non-Michaelis-Menten uptake of liposomes by the reticuloendothelial system</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>J. Pharm. Pharmacol. ,</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0022-3573</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>43</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>3</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>162 166</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1111/j.2042-7158.1991.tb06658.x</edb:english>
		</edb:article.doi>
		<edb:article.pmid>
			<edb:english>1675271</edb:english>
		</edb:article.pmid>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964337</edb:english>
		</edb:article.researchmap>
		<edb:article.author>
			<edb:english>Hideki TSUJI</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Sayoko OSAKA</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Hiroshi KIWADA</edb:english>
		</edb:article.author>
		<edb:article.title>
			<edb:english>Targeting of liposomes surface-modified with glycyrrhizin to the liver I. Preparation and biological disposition</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>Chem. Pharm. Bull. ,</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0009-2363</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>39</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>4</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>1004 1008</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1248/cpb.39.1004</edb:english>
		</edb:article.doi>
		<edb:article.pmid>
			<edb:english>1893485</edb:english>
		</edb:article.pmid>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964336</edb:english>
		</edb:article.researchmap>
		<edb:article.author>
			<edb:english>Yoko MATSUKI</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Yoshimatsu KATAKUSE</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Hiroshi MATSUURA</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Hiroshi KIWADA</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Tsuyoshi GOROMARU</edb:english>
		</edb:article.author>
		<edb:article.title>
			<edb:english>Effects of glucose and ascorbic acid on absorption and first pass metabolism of isoniazid in rats</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>Chem. Pharm. Bull. ,</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0009-2363</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>39</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>2</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>445 448</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1248/cpb.39.445</edb:english>
		</edb:article.doi>
		<edb:article.pmid>
			<edb:english>2054871</edb:english>
		</edb:article.pmid>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964308</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:english>Potential value of cetylmannoside-modified liposomes as carriers of Macrophage activators to human blood monocytes</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>Japan Journal of Cancer Research</edb:english>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>82</edb:english>
		</edb:article.volume>
		<edb:article.page>
			<edb:english>null null</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1111/j.1349-7006.1991.tb01888.x</edb:english>
		</edb:article.doi>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964306</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:english>Saturable, non-Michaelis-Menten uptake of liposomes by the retuculoendothelial System</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>Journal of Pharmacoutics and Pharmacology</edb:english>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>43</edb:english>
		</edb:article.volume>
		<edb:article.page>
			<edb:english>null null</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19910000</edb:english>
		</edb:article.date>
		<edb:article.doi>
			<edb:english>10.1111/j.2042-7158.1991.tb06658.x</edb:english>
		</edb:article.doi>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964398</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:japanese>リポソーム製剤の臨床応用は世界的にどこまで進んでいるか</edb:japanese>
		</edb:article.title>
		<edb:article.magazine>
			<edb:japanese>医学のあゆみ,</edb:japanese>
		</edb:article.magazine>
		<edb:article.volume>
			<edb:english>152</edb:english>
		</edb:article.volume>
		<edb:article.number>
			<edb:english>8</edb:english>
		</edb:article.number>
		<edb:article.page>
			<edb:english>505 null</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19900000</edb:english>
		</edb:article.date>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964401</edb:english>
		</edb:article.researchmap>
		<edb:article.title>
			<edb:japanese>リポソームを利用した体内挙動の制御</edb:japanese>
		</edb:article.title>
		<edb:article.magazine>
			<edb:japanese>生物薬剤学-最近の進歩,</edb:japanese>
		</edb:article.magazine>
		<edb:article.page>
			<edb:english>399 407</edb:english>
		</edb:article.page>
		<edb:article.date>
			<edb:english>19890000</edb:english>
		</edb:article.date>
		<edb:article.kind mapto="60752"/>
	</edb:article>
	<edb:article>
		<edb:base eid="0" eoid="0" mapto="0" mtime="0" operator="0" avail="true" censor="0" owner="60639" read="inherit" write="inherit" delete="inherit"/>
		<edb:article.researchmap>
			<edb:english>read0170980/misc/12964335</edb:english>
		</edb:article.researchmap>
		<edb:article.author>
			<edb:english>Koichiro TAHARA</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Masahiro HAYASHI</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Shoji AWAZU</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Yuriko KATO</edb:english>
		</edb:article.author>
		<edb:article.author>
			<edb:english>Hiroshi KIWADA</edb:english>
		</edb:article.author>
		<edb:article.title>
			<edb:english>Effect of serum on dose-and temperature-dependent hepatic uptake of multilamellar vesicles(MLV)</edb:english>
		</edb:article.title>
		<edb:article.magazine>
			<edb:english>J. Pharmacobio. Dyn. ,</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0386-846X</edb:english>
			</edb:article.magazine.issn>
		</edb:article.magazine>
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			<edb:english>10.1248/bpb1978.12.596</edb:english>
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			<edb:english>read0170980/misc/12964397</edb:english>
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			<edb:japanese>消化管吸収におけるドラッグデリバリーシステム</edb:japanese>
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			<edb:japanese>薬局,</edb:japanese>
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			<edb:english>read0170980/misc/12964334</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>IWAO NAKAJIMA</edb:english>
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			<edb:english>HIROSHI MATSUURA</edb:english>
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			<edb:english>MITSUKO TSUJI</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>Application of synthetic alkyl glycoside vesicles as drug carriers III. Plasma components affecting stability of the vesicles</edb:english>
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			<edb:english>read0170980/misc/12964333</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>MASAMI AKIMOTO</edb:english>
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			<edb:english>MICHIYO ARAKI</edb:english>
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			<edb:english>MITSUKO TSUJI</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>Application of synthetic liposomes based on acyl amino acids or acyl peptides as drug carriers I. Their preparation and transport of glutathione into the liver</edb:english>
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			<edb:english>read0170980/misc/12964331</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>JUNKO SATO</edb:english>
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			<edb:english>SUNJU YAMADA</edb:english>
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			<edb:english>Feasibility of magnetic liposomes as a Targeting device for drugs</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>HIROKO NISHIWAKI</edb:english>
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			<edb:english>SYNTHESIS AND EVALUATION OF A PROTOTYPAL ARTIFICIAL RED-CELL</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>HITOSHI NIIMURA</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>HITOSHI NIIMURA</edb:english>
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			<edb:english>YUICHI FUJISAKI</edb:english>
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			<edb:english>SUNJU YAMADA</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>HIROYUKI KOJIMA</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>Correlation between in vivo and in vitro dissolution rates of(α-bromoisovaleryl)urea polymorphs</edb:english>
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			<edb:english>Chem. Pharm. Bull. ,</edb:english>
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			<edb:english>32</edb:english>
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			<edb:english>19840000</edb:english>
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			<edb:english>10.1248/cpb.32.3164</edb:english>
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			<edb:english>read0170980/misc/12964310</edb:english>
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			<edb:english>Correlation between in vivo and in vitro dissolution rate of ( α-bromoisovaleryl)urea polymorphs</edb:english>
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			<edb:english>Chemical and Pharmaceutical Bulletin</edb:english>
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			<edb:english>19840000</edb:english>
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			<edb:english>10.1248/cpb.32.3164</edb:english>
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			<edb:english>read0170980/misc/12964395</edb:english>
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			<edb:japanese>リポソームII.-ドラッグキャリアーとしてのリポソーム</edb:japanese>
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			<edb:japanese>細胞工学,</edb:japanese>
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			<edb:english>Liposomes-Are they effective drug carriers?</edb:english>
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			<edb:english>19830000</edb:english>
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			<edb:english>read0170980/misc/12964324</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>HIROYUKI KOJIMA</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>Pharmacokinetic study on the polymorphs of(α-bromoisovaleryl)urea in rat</edb:english>
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			<edb:english>Chem. Pharm. Bull. ,</edb:english>
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			<edb:english>read0170980/misc/12964323</edb:english>
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			<edb:english>HIROYUKI KOJIMA</edb:english>
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			<edb:english>HITOSHI NIIMURA</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>The determination of(α-bromoisovaleryl)urea in plasma and the bioavailability of its polymorphic forms in rat</edb:english>
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			<edb:english>10.1248/cpb.30.1831</edb:english>
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			<edb:english>read0170980/misc/12964322</edb:english>
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			<edb:english>HIROYUKI KOJIMA</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>YURIKO KATO</edb:english>
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			<edb:english>The dissolution properties and physico-chemical properties of polymorphic forms of(α-bromoisovaleryl)urea</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>SHOJI AWAZU</edb:english>
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			<edb:english>MANABU HANANO</edb:english>
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			<edb:english>The study on the biological fate of paraben at the dose of practical usage in rat III. The effect of salicylic acid on the fate of paraben</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>SHOJI AWAZU</edb:english>
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			<edb:english>MANABU HANANO</edb:english>
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			<edb:english>The Study on the biological fate of paraben at the dose of practical usage in rat II. The phamacokinetic study on the blood concentration after the administration of ethyl paraben or p-hydroxybenzoic acid</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>KAZUO TAKAMI</edb:english>
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			<edb:english>The preparation and properties of a new polymorphic form of(α-bromoisovaleryl)urea</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>SHOJI AWAZU</edb:english>
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			<edb:english>The study on the biological fate of parabens at the dose of practical usage in rat I. The metabolism and excretion of ethyl-hydroxybenzoate(ethyl paraben)and p-hydroxybenzoic acid</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>TOHRU FUWA</edb:english>
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			<edb:english>HIROSHI KIWADA</edb:english>
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			<edb:english>KANAME MORITA</edb:english>
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			<edb:english>MASAHIRO HAYASHI</edb:english>
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			<edb:english>SHOJI AWAZU</edb:english>
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			<edb:english>MANABU HANANO</edb:english>
		</edb:article.author>
		<edb:article.title>
			<edb:english>A new numerical calculation method for deconvolution in linear compartment analysis of phamacokinetics.</edb:english>
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		<edb:article.magazine>
			<edb:english>Chem. Pharm. Bull. ,</edb:english>
			<edb:article.magazine.issn>
				<edb:english>0009-2363</edb:english>
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			<edb:english>25</edb:english>
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		<edb:article.number>
			<edb:english>6</edb:english>
		</edb:article.number>
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			<edb:english>1312 1318</edb:english>
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			<edb:english>19770000</edb:english>
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			<edb:english>10.1248/cpb.25.1312</edb:english>
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			<edb:english>890855</edb:english>
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			<edb:english>A new numerical calculation method for deconvolution in linear compartment analysis of pharmacokinetics</edb:english>
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		<edb:article.magazine>
			<edb:english>Chemical and Pharmaceutial Bulletin</edb:english>
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		<edb:article.volume>
			<edb:english>25</edb:english>
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			<edb:english>null null</edb:english>
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			<edb:english>10.1248/cpb.25.1312</edb:english>
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			<edb:japanese>有効性の向上とバイオアベイラビリティー</edb:japanese>
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			<edb:japanese>総合製剤学,</edb:japanese>
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			<edb:japanese>全身循環性ドラッグキャリアーは可能か?</edb:japanese>
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			<edb:japanese>生命とくすり,</edb:japanese>
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			<edb:english>Liposomes : Are they effective drug carriers?</edb:english>
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		<edb:article.publisher>
			<edb:english>Topics in Pharmaceutical Sciences 1983, ed. D. D. Breimer and P. Speiser</edb:english>
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