- Enhanced Generation of Cytotoxic T Lymphocytes by Heat Shock Protein 70 Fusion Proteins Harboring Both CD8(+) T Cell and CD4(+) T Cell Epitopes
[作者:Takemoto, S; Nishikawa, M; Guan, X; Ohno, Y; Yata, T; Takakura, Y,期刊:Molecular Pharmaceutics, 页码:1715-1723 , 文章类型: Article,,卷期:2010年7-5]
- Heat shock protein 70 (Hsp70) can be a potent carrier of antigens because it is effectively delivered to antigen presenting cells (APCs) and activates innate immunity. To induce a potent cytotoxic T lymphocyte (CTL) resp...
- Nanoparticles Based on PLGA:Poloxamer Blends for the Delivery of Proangiogenic Growth Factors
[作者:d'Angelo, I; Garcia-Fuentes, M; Parajo, Y; Welle, A; Vantus, T; Horvath, A; Bokonyi, G; Keri, G; Alonso, MJ,期刊:Molecular Pharmaceutics, 页码:1724-1733 , 文章类型: Article,,卷期:2010年7-5]
- New blood vessel formation is a critical requirement for treating many vascular and ischemia related diseases, as well as for many tissue engineering applications. Angiogenesis and vasculogenesis, in fact, represent cruc...
- Effects of PEGylation and Acetylation of PAMAM Dendrimers on DNA Binding, Cytotoxicity and in Vitro Transfection Efficiency
[作者:Fant, K; Eshjorner, EK; Jenkins, A; Grossel, MC; Lincoln, P; Norden, B,期刊:Molecular Pharmaceutics, 页码:1734-1746 , 文章类型: Article,,卷期:2010年7-5]
- Poly(amidoamine) (PAMAM) dendrimers are promising multipotent gene delivery vectors, providing favorable DNA condensation properties also in combination with the possibility of conjugation of different targeting ligands ...
- Intestinal Absorption Mechanism of Tebipenem Pivoxil, a Novel Oral Carbapenem: Involvement of Human OATP Family in Apical Membrane Transport
[作者:Kato, K; Shirasaka, Y; Kuraoka, E; Kikuchi, A; Iguchi, M; Suzuki, H; Shibasaki, S; Kurosawa, T; Tamai, I,期刊:Molecular Pharmaceutics, 页码:1747-1756 , 文章类型: Article,,卷期:2010年7-5]
- Tebipenem pivoxil (TBPM-PI) is an oral carbapenem antibiotic for treating otolaryngologic and respiratory infections in pediatric patients. This agent is a prodrug to improve intestinal absorption of TBPM, an active form...
- Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media
[作者:Fagerberg, JH; Tsinman, O; Sun, N; Tsinman, K; Avdeef, A; Bergstrom, CAS,期刊:Molecular Pharmaceutics, 页码:1419-1430 , 文章类型: Article,,卷期:2010年7-5]
- A series of poorly soluble BCS class II compounds with "grease ball" characteristics were assessed for solubility and dissolution rate in biorelevant dissolution media (BDM) with the purpose of investigating which molecu...
- Quantitative Analysis of the Effect of Supersaturation on in Vivo Drug Absorption
[作者:Takano, R; Takata, N; Saito, R; Furumoto, K; Higo, S; Hayashi, Y; Machida, M; Aso, Y; Yamashita, S,期刊:Molecular Pharmaceutics, 页码:1431-1440 , 文章类型: Article,,卷期:2010年7-5]
- The purpose of this study is to clarify the effects of intestinal drug supersaturation on solubility-limited nonlinear absorption. Oral absorption of a novel farnesyltransferase inhibitor (FTI-2600) from its crystalline ...
- Application of a Biphasic Test for Characterization of In Vitro Drug Release of Immediate Release Formulations of Celecoxib and Its Relevance to In Vivo Absorption
[作者:Shi, Y; Gao, P; Gong, YC; Ping, HL,期刊:Molecular Pharmaceutics, 页码:1458-1465 , 文章类型: Article,,卷期:2010年7-5]
- A biphasic in vitro test method was used to examine release profiles of a poorly soluble model drug, celecoxib (CEB), from its immediate release formulations. Three formulations of CEB were investigated in this study, in...
- Validation of In Vitro Cell-Based Human Blood Brain Barrier Model Using Clinical Positron Emission Tomography Radioligands To Predict In Vivo Human Brain Penetration
[作者:Mabondzo, A; Bottlaender, M; Guyot, AC; Tsaouin, K; Deverre, JR; Balimane, PV,期刊:Molecular Pharmaceutics, 页码:1805-1815 , 文章类型: Article,,卷期:2010年7-5]
- We have evaluated a novel in vitro cell-based human blood brain barrier (BBB) model that could predict in vivo human brain penetration for compounds with different BBB permeabilities using the clinical positron emission ...
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