2009
DOI: 10.1002/adma.200801808
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Mineral‐Coated Polymer Microspheres for Controlled Protein Binding and Release

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Cited by 69 publications
(93 citation statements)
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“…Such an approach was used to prepare CAP-coated PLLA microspheres with a sustained 30-day release profile of attached bovine serum albumin (BSA) in SBF compared with noncoated particles typified with an initial burst in the drug release. 349 An opposite approach, that is, coprecipitation of PLGA and a drug, tigecycline, in the presence of precursor HAP nanoparticles was recently implemented, resulting in HAP/PLGA/drug composite particles. 350 They turn out to be particularly appealing not only because of their biocompatible and biodegradable nature, but because HAP releases hydroxyl groups upon dissolution, whereas PLGA releases acidic products of degradation.…”
Section: Prospective Applicationsmentioning
confidence: 99%
“…Such an approach was used to prepare CAP-coated PLLA microspheres with a sustained 30-day release profile of attached bovine serum albumin (BSA) in SBF compared with noncoated particles typified with an initial burst in the drug release. 349 An opposite approach, that is, coprecipitation of PLGA and a drug, tigecycline, in the presence of precursor HAP nanoparticles was recently implemented, resulting in HAP/PLGA/drug composite particles. 350 They turn out to be particularly appealing not only because of their biocompatible and biodegradable nature, but because HAP releases hydroxyl groups upon dissolution, whereas PLGA releases acidic products of degradation.…”
Section: Prospective Applicationsmentioning
confidence: 99%
“…Recently, PLGA microspheres with mineral coating using a biomimetic process for controlled protein binding and release were reported. [25] In this work, particles with an average size of 150 nm formulated using polyesters such as poly(lactic acid), PCL, and PLGA are employed as templates for the CaP mineralization. The concept of using nanoparticles in general as templates for mineralization have many advantages owing to their size and high-surface area.…”
Section: Introductionmentioning
confidence: 99%
“…[73] Other recent studies of HAP/polymer composites similarly show that the presence of HAP strongly influences protein release due to protein-mineral binding. [74,75] In addition, our recent work has demonstrated that HAP-coated polymer microspheres can be used as a carrier for controlled protein binding and release, [76] and these types of microspheres can be incorporated into hydrogels to create composite-controlled release systems for drug-delivery and tissue-engineering applications. [77] The variety of processing methods available for synthesis of HAP-containing materials, coupled with the ability of HAP to bind a broad range of acidic and basic biomolecules while maintaining biological activity, indicate that biomineral-protein interactions could have broad utility in affinity-based protein delivery.…”
Section: Materials For Affinity-mediated Protein Deliverymentioning
confidence: 99%