In this paper, we present the formation of particles by self-assembly of cyclodextrin polymers and hydrophobically modified dextran followed by a controlled disruption of the particles by addition of a trigger molecule competing for the cyclodextrin cavities. The produced particles are formed from poly(vinylpyrrolidone)-co-beta-cyclodextrin and dextran-benzoate, both biocompatible polymers, and are all in the nano-/micrometer range and hence suitable for drug delivery purposes. The particle formation was studied in different ratios of poly(vinylpyrrolidone)-co-beta-cyclodextrin and dextran-benzoate by visual inspections, dynamic light scattering, isothermal titration calorimetry and SEM. The triggering of particle disruption was achieved by addition of hydroxyadamantane which has a very strong affinity towards the beta-cyclodextrin cavities. The stepwise addition of hydroxyadamantane was followed by dynamic light scattering and SEM measurements, revealing a disruption of the particles due to the addition of this competitor. These particles are believed to be promising candidates for controlled drug delivery systems, due to their unique ability to disrupt in a controlled manner. (C) 2009 Elsevier B.V. All rights reserved.
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985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
Christie, Jennifer G.
Kompella, Uday B.
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985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
985840 Nebraska Med Ctr, Dept Ophthalmol & Visual Sci, Omaha, NE 68198 USA985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Daoud-Mahammed, S.
Grossiord, J. L.
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Grossiord, J. L.
Bergua, T.
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机构:Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Bergua, T.
Amiel, C.
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CNRS, UMR 7581, Thiais, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Amiel, C.
Couvreur, P.
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Couvreur, P.
Gref, R.
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
机构:
985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
Christie, Jennifer G.
Kompella, Uday B.
论文数: 0引用数: 0
h-index: 0
机构:
985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
985840 Nebraska Med Ctr, Dept Ophthalmol & Visual Sci, Omaha, NE 68198 USA985840 Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Daoud-Mahammed, S.
Grossiord, J. L.
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h-index: 0
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Grossiord, J. L.
Bergua, T.
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h-index: 0
机构:Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Bergua, T.
Amiel, C.
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h-index: 0
机构:
CNRS, UMR 7581, Thiais, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Amiel, C.
Couvreur, P.
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h-index: 0
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France
Couvreur, P.
Gref, R.
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h-index: 0
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612, F-92290 Chatenay Malabry, France