2001
DOI: 10.1016/s0142-9612(00)00287-8
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EGF containing gelatin-based wound dressings

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Cited by 283 publications
(168 citation statements)
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“…In this view, the use of biocompatible, absorbable polymers such as pectin (Ninan et al, 2014), chitin and its derivative chitosan (Muzzarelli, 2009), gelatin (Ulubayram et al, 2001), polycaprolactone (Bui et al, 2014), hyaluronic acid (Estes et al, 1993), and others have been described.…”
Section: Figure 1 Wound Classification (Kyriacos Et Al 2008)mentioning
confidence: 99%
“…In this view, the use of biocompatible, absorbable polymers such as pectin (Ninan et al, 2014), chitin and its derivative chitosan (Muzzarelli, 2009), gelatin (Ulubayram et al, 2001), polycaprolactone (Bui et al, 2014), hyaluronic acid (Estes et al, 1993), and others have been described.…”
Section: Figure 1 Wound Classification (Kyriacos Et Al 2008)mentioning
confidence: 99%
“…There are generally two types of gelatin: Type A and Type B. Gelatin Type A is extracted and processed by acidic pretreatment of collagen, whereas gelatin Type B is obtained by alkaline pretreatment. The alkaline pretreatment converts glutamine and asparagine residues into glutamic and aspartic acids, respectively, which leads to higher carboxylic acid content for gelatin Type B than for gelatin Type A. Gelatin has several potential advantages over other natural proteins, such as its biological origin, biodegradability and commercial availability at low cost [24][25][26][27][28][29][30][31][32][33].…”
Section: Introductionmentioning
confidence: 99%
“…The wounds were excised in 5 µm thick layers under the fascia, including a 5 mm margin of unwounded skin, bisected and fixed in 10% formalin for 24 hours. The samples were processed by H&E staining for morphological observations (Li, et al 2008;Ulubayram, et al 2001). …”
Section: Histological Analysismentioning
confidence: 99%
“…A pilot study carried out in 20 diabetic patients demonstrated Herberprot ® as a feasible and safe treatment to promote the healing of chronic wounds in patients with full thickness ulcers (Fernandez-Montequin, et al 2009). However, rhEGF´s short half life requires a continuous exposure (at least 6-12 hours) to enhance the mitogenic effect on epithelial (Hardwicke, et al 2008;Ulubayram, et al 2001). Therefore, in order to achieve a significant therapeutic effect, it is necessary to optimise the administration of growth factors such as rhEGF, in terms of dose, delivery system and safety.…”
Section: Introductionmentioning
confidence: 99%