Composition for preventing or treating keloids or hypertrophic scars
a technology for hypertrophic scars and keloids, applied in the field of compositions for preventing or treating keloids or hypertrophic scars, can solve the problems of hypertrophic scars or keloids, hypertrophic scars or keloids, and limited methods, and achieve accurate diagnosis of hypertrophic scars, inhibiting the expression and activity of proteins, and preventing or treating hypertrophic scars.
Patent Information
- Authority / Receiving Office
- US · United States
- Patent Type
- Applications(United States)
- Current Assignee / Owner
- Publication Date
- 2021-12-16
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
TECHNICAL FIELD
[0001] The present invention relates to a composition for preventing or treating keloids or hypertrophic scars.BACKGROUND ART
[0002] When a dermal layer located deep in the skin is damaged due to surgery or trauma, collagen needed to maintain tension of the skin proliferates excessively in the dermal layer so that the collagen emerges from the thin skin even after a wound has healed, leaving a wound-healed scar in the skin, which is referred to “normal scar.” This appears as a result of wound healing, but hypertrophic scars or keloids may appear because fibrous tissues grow abnormally in a compact manner when the skin has a dysfunction in properly regulating and inhibiting a wound healing process. The hypertrophic scars are different from the keloids in that the hypertrophic scars do not extend beyond a wound area and tend to gradually disappear over time, but the keloids grow wider than a damaged area and penetrate into a normal skin over time. There have been various a...
Examples
Embodiment Construction
[0043]Preparation of Human Skin Fibroblasts, Normal Tissues, and Hypertrophic Scar Tissues
[0044]Skin tissues used in this experiment were obtained from a total of three patients, and an immunohistochemical (IHC) experiment was conducted using male and female normal tissues and scar tissues. Then, an effect of siRNA transformation was observed using primary fibroblast cells derived from each of the tissues.
[0045]A tissue was washed with 70% ethanol, and fats were removed by trimming. Then, the tissue was chopped to separate a tissue for the MC experiment. The remaining tissue was further trimmed, and then chopped. A mixed solution including collagenase, trypsin, and EDTA was added to the tissue, and the cells were isolated by centrifugation at 37° C. and 100 rpm. The isolated cells were cultured in an F12 medium supplanted with 10% fetal bovine serum (FBS) and gentamycin.
[0046]Comparison of Expression of Candidate Proteins Via Immunohistochemical (IHC) Experiment on Hypertrophic Scar...