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Altering macrophage and fibroblast r...

Bygd, Hannah.

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Altering macrophage and fibroblast responses with biomaterials for drug delivery, wound healing, and tissue engineering.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Altering macrophage and fibroblast responses with biomaterials for drug delivery, wound healing, and tissue engineering./
作者:	Bygd, Hannah.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:	257 p.
附註:	Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.
Contained By:	Dissertation Abstracts International77-12B(E).
標題:	Materials science. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10126496
ISBN:	9781339845364

Altering macrophage and fibroblast responses with biomaterials for drug delivery, wound healing, and tissue engineering.
Bygd, Hannah.

Altering macrophage and fibroblast responses with biomaterials for drug delivery, wound healing, and tissue engineering. - Ann Arbor : ProQuest Dissertations & Theses, 2016 - 257 p.

Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.

Thesis (Ph.D.)--Iowa State University, 2016.

Even with significant advances in the development of biomaterials for drug delivery, tissue engineering scaffolds, artificial organs, and other medical devices, one obstacle that remains is a limited understanding of material biocompatibility. Ultimately, the success or failure of these biomaterials depends on the extent of the wound healing and foreign body response following implantation. As macrophage phenotype is dynamic throughout the course of these processes, this research targets these cells to engineer improved materials for modern healthcare applications, and to better understand the material parameters that influence biocompatibility. Evidence shows that polymeric systems can influence the function of macrophages, but little progress has been made in understanding the ways in which surface chemistries and materials properties can impact macrophage differentiation and reprogramming. Controlled M1 macrophage response and increased M2 macrophage presence is of particular importance for the integration of biomaterials in to the body.

ISBN: 9781339845364Subjects--Topical Terms:

543314
Materials science.

Altering macrophage and fibroblast responses with biomaterials for drug delivery, wound healing, and tissue engineering.
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520 $a Even with significant advances in the development of biomaterials for drug delivery, tissue engineering scaffolds, artificial organs, and other medical devices, one obstacle that remains is a limited understanding of material biocompatibility. Ultimately, the success or failure of these biomaterials depends on the extent of the wound healing and foreign body response following implantation. As macrophage phenotype is dynamic throughout the course of these processes, this research targets these cells to engineer improved materials for modern healthcare applications, and to better understand the material parameters that influence biocompatibility. Evidence shows that polymeric systems can influence the function of macrophages, but little progress has been made in understanding the ways in which surface chemistries and materials properties can impact macrophage differentiation and reprogramming. Controlled M1 macrophage response and increased M2 macrophage presence is of particular importance for the integration of biomaterials in to the body.
520 $a In wound healing, polymers may also influence collagen production by fibroblast cells, which can have an impact on the quality of tissue repair and the timeliness of healing. The quality of tissue developed in wound healing is dependent on collagen organization. Random collagen deposition is found in young, healthy skin, while well-oriented collagen is typically associated with scar tissue. Achieving random collagen orientation in wound healing by exploiting biomaterial properties would be a vast improvement upon the imperfections of the natural wound healing process. This would ultimately have importance in the incorporation of implanted medical devices.
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