pH-Sensitive mPEG-Hz-Cholesterol Conjugates as a Liposome Delivery System
被引:33
作者:
Chen, Daquan
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机构:
China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Yantai Univ, Sch Pharm, Yantai 264005, Peoples R ChinaChina Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Chen, Daquan
[1
,2
]
Jiang, Xiaoqun
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机构:
Nanjing Hicin Pharmaceut Co Ltd, Nanjing 210009, Peoples R ChinaChina Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Jiang, Xiaoqun
[3
]
Huang, Yanyu
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China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R ChinaChina Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Huang, Yanyu
[1
]
Zhang, Can
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China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R ChinaChina Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Zhang, Can
[1
]
Ping, Qineng
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China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R ChinaChina Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
Ping, Qineng
[1
]
机构:
[1] China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China
[2] Yantai Univ, Sch Pharm, Yantai 264005, Peoples R China
[3] Nanjing Hicin Pharmaceut Co Ltd, Nanjing 210009, Peoples R China
Hydrazone (Hz)-based pH-sensitive methoxy(polyethylene glycol)- cholesterol conjugates (mPEG-Hz-Chol), were synthesized and used to fabricate liposomes. The structures of the mPEG2000-Hz-Chol conjugate were confirmed by FT-IR and H-1-NMR; they were stable at pH 7.4 but sensitive to mild acid conditions (pH 5.5). Plain liposomes were also prepared with S100PC/Chol, and the pH-insensitive liposomes with S100PC/Chol/mPEG2000-Chol for comparison; all the liposomes were similar in diameter similar to 20 0 nm. In vitro, the pH-sensitive liposomes released more of the model drug, paclitaxel (PTX), than the plain liposomes. The pH-sensitive liposomes were less toxic than the plain liposomes and exhibited higher cellular uptake of PTX compared with pH-insensitive liposomes by human breast cancer cells (MCF-7). The pH-sensitive mPEG2000-Hz-Chol liposomes are now being investigated as a potential new liposome drug delivery system.
机构:
Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, NetherlandsRotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Gelderblom, H
Verweij, J
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Verweij, J
Nooter, K
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Nooter, K
Sparreboom, A
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
机构:
Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, NetherlandsRotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Gelderblom, H
Verweij, J
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Verweij, J
Nooter, K
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands
Nooter, K
Sparreboom, A
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机构:Rotterdam Canc Inst, Dept Med Oncol, Daniel Den Hoed Klin, NL-3075 EA Rotterdam, Netherlands