Nanoparticle-Mediated Drug Delivery System for Cardiovascular Disease
被引:58
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作者:
Matoba, Tetsuya
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Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Fukuoka 8128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Fukuoka 8128582, Japan
Matoba, Tetsuya
[1
]
Egashira, Kensuke
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Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Fukuoka 8128582, Japan
Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Res, Fukuoka 8128582, Japan
Kyushu Univ, Grad Sch Med Sci, Dept Dev, Fukuoka 8128582, Japan
Kyushu Univ, Grad Sch Med Sci, Dept Translat Med, Fukuoka 8128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Fukuoka 8128582, Japan
Egashira, Kensuke
[1
,2
,3
,4
]
机构:
[1] Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Fukuoka 8128582, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Res, Fukuoka 8128582, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Dept Dev, Fukuoka 8128582, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Translat Med, Fukuoka 8128582, Japan
Administration of drugs and other therapeutic agents has been the central strategy of contemporary medicine for cardiovascular disease. The use of a drug delivery system (DDS) is always demanded to enhance the efficacy and safety of therapeutic agents, and improve the signal-to-noise ratio of imaging agents. Nano-scale materials modify in vivo drug kinetics, depending on (patho)physiological mechanisms such as vascular permeability and incorporation by the mononuclear phagocyte system, which constitute 'passive-targeting' properties of nano-DDS. By contrast, an 'active-targeting' strategy employs a specific targeting structure on nano-DDS, which binds to the target molecule that is specific. for a certain disease process, such as tumor specific antigens and the induction of adhesion molecules. In this review, we summarize recent studies that applied nano-DDS for the diagnosis and treatment of cardiovascular disease, especially focusing on atherosclerosis and myocardial ischemia-reperfusion (IR) injury. Pathophysiological changes in atherosclerosis and myocardial IR injury are successfully targeted by nano-DDS and preclinical studies in animals showed positive effects of nano-DDS enhancing efficacy and reducing adverse effects. The development of nano-DDS in clinical medicine is keenly being awaited.
机构:
Duquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USADuquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
Khare, Purva
Edgecomb, Sara X.
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Univ Mississippi, Dept Chem & Biochem, Oxford, MS USADuquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
Edgecomb, Sara X.
Hamadani, Christine M.
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Univ Mississippi, Dept Chem & Biochem, Oxford, MS USADuquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
Hamadani, Christine M.
Tanner, Eden E. L.
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机构:
Univ Mississippi, Dept Chem & Biochem, Oxford, MS USA
179 Coulter Hall, University, MS 38677 USADuquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
Tanner, Eden E. L.
Manickam, Devika S.
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Duquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
600 Forbes Ave,453 Mellon Hall, Pittsburgh, PA 15282 USADuquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA USA
机构:
Aston Univ, Aston Med Sch, Aston Inst Regenerat Med, Birmingham, W Midlands, England
Peking Univ, Inst Mol Med, Mol Pharmacol Lab, Beijing 100871, Peoples R ChinaSoutheast Univ, Sch Med, Zhongda Hosp, Dept Neurosurg, 87 Dingjiaqiao, Nanjing 210009, Jiangsu, Peoples R China
Gu, Yuchun
Gu, Ning
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Southeast Univ, Sch Biol Sci & Med Engn, Nanjing 210009, Jiangsu, Peoples R ChinaSoutheast Univ, Sch Med, Zhongda Hosp, Dept Neurosurg, 87 Dingjiaqiao, Nanjing 210009, Jiangsu, Peoples R China
机构:
Univ Paris 05, INSERM, UMR S 1007, UMR 8601, F-75006 Paris 06, FranceUniv Paris 06, PECSA, UPMC CNRS ESPCI ENSCP, UMR 7195, F-75252 Paris 05, France
Bombard, Sophie
Siaugue, Jean-Michel
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Univ Paris 06, PECSA, UPMC CNRS ESPCI ENSCP, UMR 7195, F-75252 Paris 05, FranceUniv Paris 06, PECSA, UPMC CNRS ESPCI ENSCP, UMR 7195, F-75252 Paris 05, France
Siaugue, Jean-Michel
Cabuil, Valerie
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Univ Paris 06, PECSA, UPMC CNRS ESPCI ENSCP, UMR 7195, F-75252 Paris 05, FranceUniv Paris 06, PECSA, UPMC CNRS ESPCI ENSCP, UMR 7195, F-75252 Paris 05, France
机构:
Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Murphy, Eric A.
Majeti, Bharat K.
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Majeti, Bharat K.
Barnes, Leo A.
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Barnes, Leo A.
Makale, Milan
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Makale, Milan
Weis, Sara M.
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Weis, Sara M.
Lutu-Fuga, Kimberly
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Lutu-Fuga, Kimberly
Wrasidlo, Wolfgang
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
Wrasidlo, Wolfgang
Cheresh, David A.
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Univ Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USAUniv Calif San Diego, Dept Pathol, Moores Canc Ctr, La Jolla, CA 92093 USA
机构:
IRCCS Azienda Osped Univ San Martino, IST Ist Nazl Ric Canc, Mutagenesis Unit, Genoa, ItalyIRCCS Azienda Osped Univ San Martino, IST Ist Nazl Ric Canc, Mutagenesis Unit, Genoa, Italy