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Temperature-responsive microcapsules

Encapsulation of PNIPAM inside non-temperature-sensitive (PSS/PAH) capsules templated on PS cores was achieved by the same ship in a bottle synthesis [37], providing temperature-responsive microcapsules. Encapsulated PNIPAM collapsed when the temperature of the system increased above 34 °C, forming discrete particles inside the capsule, without modification of the shell (Fig. 3.6). This prop-... [Pg.74]

A method to prepare well-defined responsive microcapsules and nanocapsules with engineered walls is reported. A decomposable colloidal template is coated by polyelectrolyte multilayers, and after core removal a hollow capsule, refillable with drugs, is obtained. The release of the capsule as well as mechanical properties can be tuned by adjusting pH and temperature. [Pg.91]

Poly(amino acid)s (PAAs) have also been used in drug delivery PEO-(l-aspartic acid) block copolymer nano-associates , formed by dialysis from a dimethyl acetamide solution against water, could be loaded with vasopressin. PLA-(L-lysine) block copolymer microcapsules loaded with fluorescently labelled (FITC) dextran showed release profiles dependent on amino acid content. In a nice study, poly(glutamate(OMe)-sarcosine) block copolymer particles were surface-grafted with poly(A-isopropyl acrylamide) (PNIPAAm) to produce a thermally responsive delivery system FITC-dextran release was faster below the lower critical solution temperature (LCST) than above it. PAAs are prepared by ring-opening polymerisation of A-carboxyanhydride amino acid derivatives, as shown in Scheme 1. [Pg.101]

The membranes of the thermosensitive controlled-release microcapsules were constructed by a random mixing Aquacoat (Table 1) with the latex particles having poly(EA/MMA/2-hydroxyethyl methacrylate) core and poly(A-isopropylacrylamide (NIPAAm)) shell. This is an example where the membrane has the random two-phase structure as shown in Fig. 5. The microcapsules exhibited a thermosensitive release of water-soluble drug. The mechanism is explained in Fig. 6. When the temperature was changed in a stepwise manner between 30 and 50°C, the microcapsules showed an on-off pulsatile release. This on-off response was reversible. [Pg.1777]

Figure 5.5 pH-responsive volume change ratios of PDMAEMA microcapsules prepared at different pH values. The test temperature is 37 °C. The compositions of the middle fluid are 1.0 mol DMAEMA, 0.05 mol IT MBA, 0.05% w/v V50, 1% w/v Pluronic F127, 5% w/v glycerin. (Reproduced from Wei et aiy with permission from Elsevier.)... [Pg.139]

C. Gao, S. Leporatti, S. Moya, E. Donath and H. Moehwald, Swelling and shrinking of polyelectrolyte microcapsules in response to changes in temperature and ionic strength. Chemistry — A European Journal, 9(4), 915-920 (2003). [Pg.160]


See other pages where Temperature-responsive microcapsules is mentioned: [Pg.361]    [Pg.244]    [Pg.98]    [Pg.121]    [Pg.227]    [Pg.385]    [Pg.1778]    [Pg.14]    [Pg.139]    [Pg.153]    [Pg.174]    [Pg.251]    [Pg.255]    [Pg.178]    [Pg.209]    [Pg.454]    [Pg.285]    [Pg.284]    [Pg.180]   
See also in sourсe #XX -- [ Pg.74 ]




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