Toward chronopharmaceutical drug delivery patches and biomaterial coatings for the facilitation of wound healing

被引:6
作者
Uskokovic, Vuk [1 ,2 ]
Velie, Pooja Neogi [3 ]
Wu, Victoria M. [1 ]
机构
[1] TardigradeNano LLC, Adv Mat & Nanobiotechnol Lab, Irvine, CA 92604 USA
[2] San Diego State Univ, Dept Mech Engn, San Diego, CA 92182 USA
[3] Univ Illinois, Dept Bioengn, Chicago, IL 60607 USA
关键词
Controlled drug delivery; Hydroxyapatite; Regenerative medicine; Thin film; Tissue engineering; Wound healing; POLY-L-LYSINE; IN-VITRO; CONTROLLED-RELEASE; DEGRADATION; SCAFFOLD; ACID); HYDROXYAPATITE; NANOPARTICLES; FABRICATION; HYDROGELS;
D O I
10.1016/j.jcis.2023.12.156
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Implantation of a biomaterial entails a form of injury where the integration of the implant into the host tissue greatly depends on the proper healing of the wound. Wound healing, itself, consists of a number of physiological processes, each occurring within a characteristic time window. A composite, multilayered polymeric drug de-livery carrier for adhesion to the wound site and its supply with molecules released at precise time windows at which the stages in the healing process that they target occur is conceptualized here. We also present a simplified version of one such multilayered composite fabricated by a combination of solvent casting and dip coating, comprising the base poly(epsilon-caprolactone) layer reinforced with hydroxyapatite nanoparticles, poly(glutamic acid) mesolayer and poly -L-lysine surface layer, each loaded with specific small molecules and released at moderately distinct timescales, partially matching the chronology of wound healing. To that end, the base layer proved suitable for the delivery of an anti-inflammatory molecule or an angiogenic agent, the mesolayer appeared appropriate for the delivery of an epithelialization promoter or a granulation factor, and the adhesive surface layer interfacing directly with the site of injury showed promise as a carrier of a vasodilator. The drug release mechanisms were diffusion-driven, suggesting that the drug/carrier interaction is a key determinant of the release kinetics, as important as the nature of the polymer and its hydrolytic degradation rate in the aqueous medium. Morphological and phase composition analyses were performed, along with the cell compatibility ones, demonstrating solid adhesion and proliferation of both transformed and primary fibroblasts on both surfaces of the composite films. The design of the multilayered composite drug delivery carriers presented here is prospective, but requires further upgrades to achieve the ideal of a perfect timing of the sequential drug release kinetics and a perfect resonance with the physiological processes defining the chronology of wound healing.
引用
收藏
页码:355 / 363
页数:9
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