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Biomedical subjects

Chien-Chi Lin

Publications and source records attributed to Chien-Chi Lin.

3 recordsLinked to original sources

Hydrogels in controlled release formulations: network design and mathematical modeling.

Over the past few decades, advances in hydrogel technologies have spurred development in many biomedical applications including controlled drug delivery. Many novel hydrogel-based delivery matrices have been designed and fabricated to fulfill the ever-increasing needs of the pharmaceutical and medical fields. Mathematical modeling plays an important role in facilitating hydrogel network design by identifying key parameters and molecule release mechanisms. The objective of this article is to review the fundamentals and recent advances in hydrogel network design as well as mathematical modeling approaches related to controlled molecule release from hydrogels. In the first section, the niche roles of hydrogels in controlled release, molecule release mechanisms, and hydrogel design criteria for controlled release applications are discussed. Novel hydrogel systems for drug delivery including biodegradable, smart, and biomimetic hydrogels are reviewed in the second section. Several mechanisms have been elucidated to describe molecule release from polymer hydrogel systems including diffusion, swelling, and chemically-controlled release. The focus of the final part of this article is discussion of emerging hydrogel delivery systems and challenges associated with modeling the performance of these devices.

Chemistry, Pharmaceutical↗

Enhanced protein delivery from photopolymerized hydrogels using a pseudospecific metal chelating ligand.

PURPOSE: This study was conducted to investigate the cause of incomplete protein release from photopolymerized poly(ethylene glycol) (PEG) hydrogels and verify the protein-protection mechanism provided by iminodiacetic acid (IDA). METHODS: The in vitro release of bovine serum albumin (BSA) from PEG hydrogels prepared under different conditions was studied. Photoinitiator and initial protein concentrations were varied as well as the addition of IDA and metal ions. Protein immobilization within the nondegradable networks via free-radical reaction was demonstrated by gel electrophoresis. RESULTS: Protein release efficiency was shown to be dependent on photoinitiator and initial protein concentration. Gel electrophoresis results revealed immobilization of protein to the polymer network and further indicated the detrimental role of free radicals in lowering protein-release efficiency. Adding IDA to the prepolymer solution enhanced total protein release from the subsequently photopolymerized network in a dose-dependent manner. The addition of metal ions including Cu2+, Zn2+, and Ni2+ further increased BSA release efficiency. Agreement between the protein release data and theoretical model predictions accounting for reversible protein-IDA binding further validated the protection effect provided by IDA and IDA-transition metal complexes. CONCLUSIONS: The protection effect described in this study offers a novel strategy for increasing the delivery efficiencies of many therapeutically valuable proteins.

Chelating Agents↗

Micropatterning proteins and cells on polylactic acid and poly(lactide-co-glycolide).

Techniques for micropatterning proteins and cells on biomaterials are important in tissue engineering applications. Here, we present a method for patterning proteins and cells on poly(lactic acid) (PLA) and poly(lactide-co-glycolide) (PLGA) substrates that are routinely used as scaffolds in engineering tissues. Poly(oligoethyleneglycol methacrylate) (poly-OEGMA) or poly(oligoethyleneglycol methacrylate-co-methacrylic acid) (poly(OEGMA-co-MA)) was microcontact printed onto substrates to create cell resistant areas. Proteins adsorbed onto the unprinted regions whereas the polymer printed regions effectively repel non-specific protein adsorption. NIH 3T3 fibroblasts remain confined within the patterns on the PLGA and PLA films for up to 2 weeks and aligned their actin cytoskeleton along the line patterns. In comparison to unpatterned cells, fibroblasts confined within line-shaped patterns show fewer actin filaments. This method for controlling the spatial morphology and distribution of cells on synthetic biomaterials could have significant applications in tissue engineering.

Adsorption↗