TWI538695B - Manufacturing method of dressing - Google Patents

Manufacturing method of dressing Download PDF

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TWI538695B
TWI538695B TW103118446A TW103118446A TWI538695B TW I538695 B TWI538695 B TW I538695B TW 103118446 A TW103118446 A TW 103118446A TW 103118446 A TW103118446 A TW 103118446A TW I538695 B TWI538695 B TW I538695B
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fiber membrane
glycerin
bacterial fiber
bacterial
dressing
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TW103118446A
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TW201544127A (en
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許惠如
李瑞生
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財團法人紡織產業綜合研究所
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Description

敷材的製造方法 Method for manufacturing a material

本發明是有關於一種敷材的製造方法,且特別是有關於一種細菌纖維敷材的製造方法。 The present invention relates to a method of producing a dressing material, and more particularly to a method of manufacturing a bacterial fiber dressing.

細菌纖維膜(bacterial cellulose film,BC film)是微生物經發酵培養後所形成不溶於水且堅韌的緻密水膠膜,其主要由纖維素與水構成,且其水分含量可超過90%。細菌纖維膜之化學結構與天然纖維素相同,故可廣泛地應用於例如燙傷敷材與面膜基材上。 Bacterial cellulose film (BC film) is a water-insoluble and tough dense water film formed by fermentation of microorganisms. It is mainly composed of cellulose and water, and its moisture content can exceed 90%. The bacterial fiber membrane has the same chemical structure as natural cellulose, and thus can be widely applied to, for example, scald dressings and mask substrates.

相較於一般的不織布基材面膜產品,細菌纖維膜產品受到微生物污染之機會相對較高。一般而言,為了確保細菌纖維膜產品的使用安全性,會提高產品中防腐劑的添加濃度。然而,高含量的防腐劑可能對皮膚造成刺激。為了解決這個問題,細菌纖維膜產品的另一種保存方式是將其於低溫(冷凍)下保存。 Bacterial fiber membrane products are relatively more susceptible to microbial contamination than conventional non-woven substrate mask products. In general, in order to ensure the safety of the use of the bacterial fiber membrane product, the concentration of the preservative added to the product is increased. However, high levels of preservatives may cause irritation to the skin. To solve this problem, another way to preserve bacterial fiber membrane products is to store them at low temperatures (freezing).

然而,雖然冷凍可解決上述防腐劑添加之問題,但細菌纖維膜產品中的水分卻會在冷凍降溫的過程中析出於纖維膜表 面。尤其當冷凍過程的環境溫度不夠低而無法快速冷凍產品時,水分析出的影響更為顯著。因此,亟需一種具有較低凝固溫度的細菌纖維膜。 However, although freezing can solve the above problem of preservative addition, the moisture in the bacterial fiber membrane product will precipitate out of the fiber membrane during the freezing and cooling process. surface. Especially when the ambient temperature of the freezing process is not low enough to quickly freeze the product, the effect of water analysis is more pronounced. Therefore, there is a need for a bacterial fiber membrane having a lower solidification temperature.

本發明提供一種敷材的製造方法,其可製造出耐低溫、解凍快、冰凍解凍重量變化率小的敷材。 The present invention provides a method for producing a dressing material which can produce a dressing material which is resistant to low temperature, quick thawing, and low in freeze thawing weight change rate.

本發明提出一種敷材的製造方法,其包括以下的步驟。首先,提供細菌纖維膜,此細菌纖維膜包括細菌纖維素與水分。接著,將細菌纖維膜浸置於甘油水溶液中,並加熱至大於100℃,以使甘油水溶液之甘油置換細菌纖維膜中之水分。之後,進行透析程序,其中透析程序之溫度低於室溫,以使甘油於細菌纖維膜中呈現濃度梯度分布。 The present invention provides a method of manufacturing a dressing comprising the following steps. First, a bacterial fiber membrane is provided, which includes bacterial cellulose and moisture. Next, the bacterial fiber membrane is immersed in an aqueous glycerin solution and heated to more than 100 ° C to replace the glycerin in the aqueous glycerin solution with the water in the bacterial fiber membrane. Thereafter, a dialysis procedure is performed in which the temperature of the dialysis procedure is below room temperature such that glycerol exhibits a concentration gradient distribution in the bacterial fiber membrane.

在本發明的一實施例中,上述的細菌纖維膜的厚度是D,且舉例而言,D≧2mm。 In an embodiment of the invention, the thickness of the bacterial fiber membrane described above is D, and for example, D ≧ 2 mm.

在本發明的一實施例中,上述的敷材的製造方法中,以甘油水溶液的總重量計,甘油水溶液之甘油的含量例如是50重量%至80重量%。 In an embodiment of the present invention, in the method for producing a cast material, the content of glycerin in the aqueous glycerin solution is, for example, 50% by weight to 80% by weight based on the total weight of the aqueous glycerin solution.

在本發明的一實施例中,上述的敷材的製造方法中,透析程序之溫度為T,且T例如滿足0℃<T≦26℃。 In an embodiment of the present invention, in the method for producing a veneer, the temperature of the dialysis program is T, and T satisfies, for example, 0 ° C < T ≦ 26 ° C.

在本發明的一實施例中,上述的敷材的製造方法中,透析程序之溫度為T,且T例如滿足0℃<T≦10℃。 In an embodiment of the present invention, in the method for producing a cast material, the temperature of the dialysis program is T, and T satisfies, for example, 0 ° C < T ≦ 10 ° C.

在本發明的一實施例中,上述的敷材的製造方法中,透析程序之時間例如是介於0小時至24小時之間。 In an embodiment of the invention, in the method of manufacturing the above-mentioned dressing, the time of the dialysis procedure is, for example, between 0 hours and 24 hours.

在本發明的一實施例中,上述的敷材的製造方法中,細菌纖維膜包括表層以及中心處,且呈現濃度梯度分布之甘油之濃度自細菌纖維膜之表層至中心處遞增。 In an embodiment of the present invention, in the method for producing a cast material, the bacterial fiber membrane includes a surface layer and a center, and a concentration of glycerin exhibiting a concentration gradient distribution increases from a surface layer to a center of the bacterial fiber membrane.

在本發明的一實施例中,上述的敷材的製造方法中,以細菌纖維膜的總重量計,呈現濃度梯度分布之甘油的平均甘油含量例如是20重量%至60重量%。 In an embodiment of the present invention, in the method for producing a cast material, the average glycerin content of the glycerin exhibiting a concentration gradient distribution is, for example, 20% by weight to 60% by weight based on the total weight of the bacterial fiber membrane.

在本發明的一實施例中,上述的敷材的製造方法中,細菌纖維素之纖維直徑為20nm至100nm。 In an embodiment of the invention, in the method for producing a cast material, the bacterial cellulose has a fiber diameter of 20 nm to 100 nm.

在本發明的一實施例中,上述的敷材的製造方法更包括以下的步驟:進行冷凍程序,其中冷凍程序之溫度小於0℃且大於-14℃。接著,進行解凍程序,其中解凍程序之時間為10分鐘至20分鐘。 In an embodiment of the invention, the method of manufacturing the above-described dressing further comprises the step of performing a freezing process wherein the temperature of the freezing process is less than 0 ° C and greater than -14 ° C. Next, a thawing procedure is performed in which the thawing procedure is performed for 10 minutes to 20 minutes.

基於上述,本發明之敷材的製造方法的製程簡單,且可製造出耐低溫、解凍快、冰凍解凍重量變化率小的敷材。 Based on the above, the manufacturing method of the dressing material of the present invention has a simple process, and can produce a dressing material which is resistant to low temperature, quick thawing, and low in freezing and thawing weight change rate.

為讓本發明的上述特徵和優點能更明顯易懂,下文特舉實施例,並配合所附圖式作詳細說明如下。 The above described features and advantages of the invention will be apparent from the following description.

10‧‧‧表層 10‧‧‧ surface

20‧‧‧中心處 20‧‧‧ Center

S110、S120、S130‧‧‧步驟 S110, S120, S130‧‧‧ steps

圖1為本發明之一實施例之敷材的製造流程示意圖。 1 is a schematic view showing a manufacturing process of a dressing material according to an embodiment of the present invention.

圖2為本發明之一實施例之敷材的立體示意圖。 2 is a perspective view of a dressing material according to an embodiment of the present invention.

圖3為本發明之一實施例之敷材的甘油濃度梯度曲線圖。 Figure 3 is a graph showing the glycerin concentration gradient of a dressing according to an embodiment of the present invention.

圖1為本發明之一實施例之敷材的製造流程示意圖。請 參照圖1,首先,進行步驟S110,提供細菌纖維膜。詳細而言,細菌纖維膜例如是將醋酸菌靜置培養所產生的緻密水膠膜,然本發明不限於此。細菌纖維膜包括纖維素與水分。值得一提的是,本實施例之細菌纖維膜可利用培養方式先產生非純化的細菌纖維膜,再經鹼液鹼洗的程序後,得到純度較高的細菌纖維膜。上述鹼液可以選自氫氧化鈉、次氯酸鈉或碳酸氫鈉,然本發明不限於此。此外,上述細菌纖維膜具有緻密孔洞結構以及良好的拉伸強度,且細菌纖維素之纖維直徑例如為20nm至100nm,然本發明不限於此。 1 is a schematic view showing a manufacturing process of a dressing material according to an embodiment of the present invention. please Referring to Fig. 1, first, step S110 is performed to provide a bacterial fiber membrane. Specifically, the bacterial fiber membrane is, for example, a dense water gel film produced by static culture of acetic acid bacteria, but the present invention is not limited thereto. Bacterial fiber membranes include cellulose and water. It is worth mentioning that the bacterial fiber membrane of the present embodiment can produce a non-purified bacterial fiber membrane by a culture method, and then obtain a high purity bacterial fiber membrane by a lye alkaline washing procedure. The above lye may be selected from sodium hydroxide, sodium hypochlorite or sodium hydrogencarbonate, but the invention is not limited thereto. Further, the above bacterial fiber membrane has a dense pore structure and good tensile strength, and the fiber diameter of the bacterial cellulose is, for example, 20 nm to 100 nm, but the present invention is not limited thereto.

接著,進行步驟S120,將細菌纖維膜浸置於甘油水溶液中,並加熱20分鐘左右,使溫度升高至大於100℃。在本實施例中,以甘油水溶液的總重量計,甘油水溶液之甘油的含量例如是50重量%至80重量%。此步驟為溶液置換程序,以使甘油水溶液之甘油均勻地導入細菌纖維膜中。一般常用的抗凍劑例如為甲醇、乙醇、乙二醇、甘油、水溶性醯胺、氯化鈣、鹽水等。由於甘油無毒性而安全性高,故本實施例較佳是使用甘油來降低細菌纖維膜之凝固溫度。 Next, in step S120, the bacterial fiber membrane is immersed in an aqueous glycerin solution and heated for about 20 minutes to raise the temperature to more than 100 °C. In the present embodiment, the glycerin content of the aqueous glycerin solution is, for example, 50% by weight to 80% by weight based on the total weight of the aqueous glycerin solution. This step is a solution replacement procedure in which glycerin of an aqueous glycerin solution is uniformly introduced into the bacterial fiber membrane. Commonly used antifreeze agents are, for example, methanol, ethanol, ethylene glycol, glycerin, water-soluble guanamine, calcium chloride, salt water, and the like. Since glycerin is non-toxic and highly safe, this embodiment preferably uses glycerin to lower the solidification temperature of the bacterial fiber membrane.

特別的是,在本實施例中,細菌纖維膜的厚度為D,且舉例而言,D≧2mm,且D較佳例如是介於2.0mm至5.0mm。一般而言,常用的溶液置換為浸置方式。然而,單純浸置方式之溶液置換效果常受限於時間、細菌纖維膜的厚度與置換溶液的濃度。尤其是,當細菌纖維膜的厚度D達到一定的厚度(例如2mm)以上時,上述浸置方式就只能使甘油擴散至細菌纖維膜的表層,而無法擴散進入細菌纖維膜的內部。如此一來,將導致敷材的表層具有較高含量的甘油,而這可能使得皮膚的水分被敷材表層的高含量甘油所吸走,進而造成使用者皮膚乾燥的問題。相較之下,本實施例之敷材的製造方法是藉由加熱至大於100℃的方式,並利用甘油與水之間的沸點差異來達到置換的目的。如此一來,可使甘油完全取代細菌纖維膜中的水分,並可均勻地散佈於具有一定厚度的細菌纖維膜中,此外,此置換方式也不會影響細菌纖維膜的結構。 In particular, in the present embodiment, the thickness of the bacterial fiber membrane is D, and for example, D ≧ 2 mm, and D is preferably, for example, 2.0 mm to 5.0 mm. In general, the usual solution replacement is an immersion method. However, the solution displacement effect of the simple immersion method is often limited by the time, the thickness of the bacterial fiber membrane, and the concentration of the replacement solution. In particular, when the thickness D of the bacterial fiber membrane reaches a certain thickness (for example, 2 mm) or more, the above-described immersion method can only diffuse glycerin to the surface layer of the bacterial fiber membrane and cannot diffuse into the interior of the bacterial fiber membrane. As a result, the surface layer of the dressing will have a higher content of glycerin, which may cause the moisture of the skin to be absorbed by the high content of glycerin on the surface layer of the dressing, thereby causing the problem of dry skin of the user. In contrast, the method of manufacturing the dressing of the present embodiment achieves the purpose of replacement by heating to a temperature greater than 100 ° C and utilizing the difference in boiling point between glycerin and water. In this way, the glycerin can completely replace the moisture in the bacterial fiber membrane, and can be uniformly dispersed in the bacterial fiber membrane having a certain thickness, and the substitution manner does not affect the structure of the bacterial fiber membrane.

再來,進行步驟S130,於低於室溫的溫度下進行透析程序,以使甘油於細菌纖維膜中呈現濃度梯度分布。在本實施例中,透析程序之溫度為T,且T較佳滿足0℃<T≦26℃,T更佳滿足0℃<T≦10℃。在上述溫度範圍內,甘油呈黏稠狀而擴散較慢,故有利於甘油濃度梯度的形成。在本實施例中,透析程序之時間例如是介於0小時至24小時之間。 Further, in step S130, a dialysis procedure is performed at a temperature lower than room temperature to cause glycerol to exhibit a concentration gradient distribution in the bacterial fiber membrane. In the present embodiment, the temperature of the dialysis program is T, and T preferably satisfies 0 ° C < T ≦ 26 ° C, and T more preferably satisfies 0 ° C < T ≦ 10 ° C. In the above temperature range, glycerin is viscous and diffuses slowly, which is beneficial to the formation of a glycerol concentration gradient. In the present embodiment, the time of the dialysis procedure is, for example, between 0 hours and 24 hours.

圖2為本發明之一實施例之敷材的立體示意圖。請參照圖2,細菌纖維膜包括表層10以及中心處20,且呈現濃度梯度分 布之甘油之濃度自細菌纖維膜之表層10至中心處20遞增。在本實施例中,以細菌纖維膜的總重量計,呈現濃度梯度分布之甘油的平均甘油含量例如是20重量%至60重量%。圖3為本發明之一實施例之敷材的甘油濃度梯度曲線圖。請同時參照圖2與圖3,以敷材的中心處20當作0mm,橫軸為自中心處20至表層10方向的距離(mm),距離愈大表示愈接近敷材之表層10。縱軸為呈現濃度梯度分布之甘油含量(重量%)。請參照圖3,經過上述透析程序後之敷材的甘油濃度梯度是自細菌纖維膜之表層10至中心處20遞增。由於細菌纖維膜接近中心處20具有較高濃度的甘油,故於冷凍後其內部不會結冰。如此一來,可降低本實施例之敷材解凍後之外觀變化程度,並可減少敷材的解凍時間以及保有其釋水功能。 2 is a perspective view of a dressing material according to an embodiment of the present invention. Referring to FIG. 2, the bacterial fiber membrane includes a surface layer 10 and a center portion 20, and exhibits a concentration gradient. The concentration of glycerin in the cloth increases from the surface 10 to the center 20 of the bacterial fiber membrane. In the present embodiment, the average glycerin content of the glycerin exhibiting a concentration gradient distribution is, for example, 20% by weight to 60% by weight based on the total weight of the bacterial fiber membrane. Figure 3 is a graph showing the glycerin concentration gradient of a dressing according to an embodiment of the present invention. Referring to FIG. 2 and FIG. 3 simultaneously, the center 20 of the material is regarded as 0 mm, and the horizontal axis is the distance (mm) from the center 20 to the surface layer 10. The larger the distance, the closer to the surface layer 10 of the material. The vertical axis is the glycerin content (% by weight) exhibiting a concentration gradient distribution. Referring to Figure 3, the glycerin concentration gradient of the dressing after the above dialysis procedure is increased from the surface 10 to the center 20 of the bacterial fiber membrane. Since the bacterial fiber membrane has a higher concentration of glycerin near the center 20, it does not freeze inside after freezing. In this way, the degree of appearance change after the thawing of the dressing of the embodiment can be reduced, and the thawing time of the dressing material and the function of releasing the water can be reduced.

值得一提的是,一般細菌纖維膜經冷凍解凍程序後,膜材所含之水分會因為冰晶形成而造成膜材水分受擠壓而析出膜材外,導致細菌纖維膜於冷凍解凍後膜材外觀受到影響。相較之下,由於本實施例之敷材含有呈濃度梯度的甘油,故可改善上述水分析出的現象,而有助於提升冷凍解凍程序後之重量回復率。 It is worth mentioning that after the freezing and thawing process of the bacterial fiber membrane, the moisture contained in the membrane will cause the membrane water to be squeezed out due to the formation of ice crystals, which will cause the membrane of the membrane to be frozen and thawed. The appearance is affected. In contrast, since the dressing of the present embodiment contains glycerin having a concentration gradient, the above-described phenomenon of water analysis can be improved, and the weight recovery rate after the freezing and thawing process can be improved.

敷材之特性評價Evaluation of the characteristics of the material

以下將列舉數個比較例與實驗例來說明本實施例之敷材的抗凍性、解凍時間、冷凍解凍重量回復率與釋水效能。 Hereinafter, several comparative examples and experimental examples will be described to illustrate the freeze resistance, thawing time, freeze thawing weight recovery rate and water release efficiency of the dressing of the present embodiment.

[抗凍性] [freezing resistance]

詳細而言,抗凍性的評價方式為將比較例與實驗例之樣 品於-14℃下保存24小時後,觀察其有無結凍的現象,將其結果列於表一。 In detail, the evaluation method of frost resistance is the same as the comparative example and the experimental example. After storage for 14 hours at -14 ° C, the presence or absence of freezing was observed, and the results are shown in Table 1.

[解凍時間] [thaw time]

詳細而言,解凍速率的評價方式為將上述於-14℃下保存24小時後之比較例與實驗例的樣品,將其移至室溫下解凍,並量測其完全解凍所需的時間,將其結果列於表一。 Specifically, the thawing rate is evaluated by the above-mentioned sample of the comparative example and the experimental example after storage at -14 ° C for 24 hours, which is then thawed at room temperature, and the time required for complete thawing is measured, The results are listed in Table 1.

[重量回復率] [weight recovery rate]

詳細而言,將比較例與實驗例之樣品於-14℃下保存24小時,量測其重量Wa。隨後,將其移至室溫下解凍,量測其重量Wb。本文中,以冷凍解凍重量回復率(%)來量化冷凍解凍後敷材之外觀變化。重量回復率(%)的定義為:Wb/Wa×100%,其中Wa為冷凍解凍前之敷材重量(mg),Wb為冷凍解凍後之敷材重量(mg),將其結果列於表一。重量回復率愈高,表示敷材之外觀變化愈小。 Specifically, the samples of the comparative examples and the experimental examples were stored at -14 ° C for 24 hours, and the weight Wa was measured. Subsequently, it was thawed at room temperature, and its weight Wb was measured. Herein, the freeze-thaw weight recovery rate (%) is used to quantify the appearance change of the frozen-thawed dressing. The weight recovery rate (%) is defined as: Wb/Wa × 100%, where Wa is the weight (mg) of the material before freezing and thawing, and Wb is the weight (mg) of the material after freezing and thawing, and the results are listed in the table. One. The higher the weight recovery rate, the smaller the change in appearance of the dressing.

[釋水效能] [Water release efficiency]

詳細而言,利用65重量%之明膠膜來模擬人體皮膚,將比較例與實驗例之樣品置於明膠膜上15分鐘後,比較明膠片之重量變化差異。釋水效能(%)的定義為:實驗例之明膠重量變化(mg)/比較例2之明膠重量變化(mg)/×100%,將其結果列於表一。 Specifically, a 65% by weight gelatin film was used to simulate human skin, and a comparative sample and a sample of the experimental example were placed on a gelatin film for 15 minutes, and the difference in weight change of the film was compared. The water release efficiency (%) was defined as the gelatin weight change (mg) of the experimental example/the gelatin weight change (mg)/×100% of Comparative Example 2, and the results are shown in Table 1.

比較例1為市售果凍面膜,比較例2為不含甘油之細菌纖維膜。實驗例1為平均甘油含量>90重量%之細菌纖維膜,實驗例2為平均甘油含量為60重量%之細菌纖維膜,實驗例3為平均甘油含量為40重量%之細菌纖維膜,實驗例4為平均甘油含量為20重量%之細菌纖維膜,實驗例5為平均甘油含量為10重量%之細菌纖維膜。應注意,實驗例1至實驗例5的細菌纖維膜皆於4℃進行透析程序。 Comparative Example 1 is a commercially available jelly mask, and Comparative Example 2 is a bacterial fiber membrane containing no glycerin. Experimental Example 1 is a bacterial fiber membrane having an average glycerin content of >90% by weight, Experimental Example 2 is a bacterial fiber membrane having an average glycerin content of 60% by weight, and Experimental Example 3 is a bacterial fiber membrane having an average glycerin content of 40% by weight, Experimental Example 4 is a bacterial fiber membrane having an average glycerin content of 20% by weight, and Experimental Example 5 is a bacterial fiber membrane having an average glycerin content of 10% by weight. It should be noted that the bacterial fiber membranes of Experimental Examples 1 to 5 were subjected to a dialysis procedure at 4 °C.

由表一的結果可知,當本實施例之敷材中的平均甘油濃度高於60重量%時(即實驗例1與實驗例2),則其於0℃至-14℃的環境中仍可長時間維持濕潤狀態而不會結冰。然而,若欲將敷材應用於例如面膜之皮膚敷料,則除了考慮敷材產品之耐低溫性之外,還需保留產品的釋水效能。基於綜合因素的考量,敷材中的平均甘油濃度較佳的範圍為:10重量%<平均甘油濃度≦40重量%(即實驗例3與實驗例4)。具體而言,當敷材的平均甘油濃度落於上述範圍內時,雖然敷材會結凍,然其解凍後的重量回復率≧83%,且解凍時間短(≦10分鐘)。值得一提的是,實驗例3與實 驗例4之敷材還可同時保有良好的釋水效能,其分別為69.6%與71.9%。 From the results of Table 1, it can be seen that when the average glycerin concentration in the dressing of the present embodiment is higher than 60% by weight (ie, Experimental Example 1 and Experimental Example 2), it is still in the environment of 0 ° C to -14 ° C. Maintain a wet state for a long time without freezing. However, if the dressing is to be applied to a skin dressing such as a mask, in addition to considering the low temperature resistance of the dressing product, it is necessary to retain the water release efficiency of the product. Based on the consideration of the comprehensive factors, the average glycerin concentration in the dressing is preferably in the range of 10% by weight < average glycerin concentration ≦ 40% by weight (ie, Experimental Example 3 and Experimental Example 4). Specifically, when the average glycerin concentration of the dressing falls within the above range, although the dressing material is frozen, the weight recovery rate after thawing is ≧83%, and the thawing time is short (≦10 minutes). It is worth mentioning that the experimental example 3 and the real The dressing of the test case 4 can also maintain a good water release efficiency, which is 69.6% and 71.9%, respectively.

另外,為了說明溫度對透析程序效果的影響,以下列舉數個實驗例加以說明。實驗例1為於1℃進行透析程序之細菌纖維膜,實驗例2為於4℃進行透析程序之細菌纖維膜,實驗例3為於10℃進行透析程序之細菌纖維膜。應注意,於實驗例1至實驗例3的細菌纖維膜中的平均甘油含量皆為40重量%。其結果列於表二。 Further, in order to explain the influence of temperature on the effect of the dialysis program, several experimental examples are described below. Experimental Example 1 is a bacterial fiber membrane subjected to a dialysis procedure at 1 ° C, Experimental Example 2 is a bacterial fiber membrane subjected to a dialysis procedure at 4 ° C, and Experimental Example 3 is a bacterial fiber membrane subjected to a dialysis procedure at 10 ° C. It should be noted that the average glycerin content in the bacterial fiber membranes of Experimental Examples 1 to 3 was 40% by weight. The results are shown in Table 2.

由表二的結果可知,隨著進行透析程序時的溫度提升,敷材之釋水效能也會增加。具體而言,於10℃進行透析程序之敷材可具有較佳的釋水效能(達75.4%)。應注意,溫度愈低,透析程序所需的時間愈多。舉例而言,於10℃進行透析程序的平衡時間約1小時至2小時,而於1℃進行透析程序的平衡時間約2小時至3小時。 As can be seen from the results in Table 2, as the temperature during the dialysis procedure increases, the water release efficiency of the dressing increases. In particular, the dressings subjected to the dialysis procedure at 10 ° C may have better water release performance (up to 75.4%). It should be noted that the lower the temperature, the more time is required for the dialysis procedure. For example, the equilibration time of the dialysis procedure at 10 ° C is about 1 hour to 2 hours, while the equilibrium time of the dialysis procedure at 1 ° C is about 2 hours to 3 hours.

綜上所述,本發明利用甘油的抗凍特性,透過加熱方式的溶液置換程序來將甘油均勻導入細菌纖維膜中,再藉由透析程序來控制細菌纖維膜中的甘油濃度以形成濃度梯度,從而製造可耐低溫、解凍快且冰凍解凍重量變化率小的敷材。如此一來,本發明之敷材可適合於低溫下保存,而無須添加高濃度的防腐劑。 In summary, the present invention utilizes the antifreeze property of glycerin, and uniformly introduces glycerin into the bacterial fiber membrane through a heating solution replacement procedure, and then controls the concentration of glycerol in the bacterial fiber membrane to form a concentration gradient by a dialysis procedure. Thereby, a veneer which is resistant to low temperature, quick thawing and has a small rate of change in freeze thawing weight is produced. In this way, the dressing of the present invention can be suitably stored at low temperatures without the need to add a high concentration of preservative.

雖然本發明已以實施例揭露如上,然其並非用以限定本發明,任何所屬技術領域中具有通常知識者,在不脫離本發明的精神和範圍內,當可作些許的更動與潤飾,故本發明的保護範圍當視後附的申請專利範圍所界定者為準。 Although the present invention has been disclosed in the above embodiments, it is not intended to limit the present invention, and any one of ordinary skill in the art can make some changes and refinements without departing from the spirit and scope of the present invention. The scope of the invention is defined by the scope of the appended claims.

S110、S120、S130‧‧‧步驟 S110, S120, S130‧‧‧ steps

Claims (8)

一種敷材的製造方法,包括:提供一細菌纖維膜,包括細菌纖維素與水分;將該細菌纖維膜浸置於一甘油水溶液中,並加熱至大於100℃,以使該甘油水溶液之甘油完全置換該細菌纖維膜中之該水分,其中以該甘油水溶液的總重量計,該甘油水溶液之該甘油的含量為50重量%至80重量%;以及進行一透析程序,其中該透析程序之溫度為T,且T滿足0℃<T≦26℃,以使該甘油於該細菌纖維膜中呈現濃度梯度分布。 A method for manufacturing a dressing comprising: providing a bacterial fiber membrane comprising bacterial cellulose and moisture; immersing the bacterial fiber membrane in an aqueous solution of glycerin and heating to greater than 100 ° C to complete the glycerin of the aqueous glycerin solution Displace the moisture in the bacterial fiber membrane, wherein the glycerin content of the glycerin aqueous solution is 50% by weight to 80% by weight based on the total weight of the glycerin aqueous solution; and performing a dialysis procedure, wherein the temperature of the dialysis procedure is T, and T satisfies 0 ° C < T ≦ 26 ° C, so that the glycerol exhibits a concentration gradient distribution in the bacterial fiber membrane. 如申請專利範圍第1項所述之敷材的製造方法,其中該細菌纖維膜的厚度為D,且D≧2mm。 The method for producing a dressing according to claim 1, wherein the bacterial fiber membrane has a thickness D and a D ≧ 2 mm. 如申請專利範圍第1項所述之敷材的製造方法,其中該透析程序之溫度為T,且T滿足0℃<T≦10℃。 The method for producing a dressing according to claim 1, wherein the temperature of the dialysis program is T, and T satisfies 0 ° C < T ≦ 10 ° C. 如申請專利範圍第1項所述之敷材的製造方法,其中該透析程序之時間介於0至24小時之間。 The method of manufacturing a dressing according to claim 1, wherein the dialysis procedure is between 0 and 24 hours. 如申請專利範圍第1項所述之敷材的製造方法,其中該細菌纖維膜包括一表層以及一中心處,且呈現濃度梯度分布之該甘油之濃度自該細菌纖維膜之該表層至該中心處遞增。 The method for producing a dressing according to claim 1, wherein the bacterial fiber membrane comprises a surface layer and a center, and the concentration of the glycerin exhibiting a concentration gradient distribution is from the surface layer of the bacterial fiber membrane to the center Increase. 如申請專利範圍第1項所述之敷材的製造方法,其中以該細菌纖維膜的總重量計,呈現濃度梯度分布之該甘油的平均甘油含量為20重量%至60重量%。 The method for producing a dressing according to claim 1, wherein the glycerin exhibiting a concentration gradient distribution has an average glycerin content of from 20% by weight to 60% by weight based on the total weight of the bacterial fiber membrane. 如申請專利範圍第1項所述之敷材的製造方法,其中該細 菌纖維素之纖維直徑為20nm至100nm。 The method for manufacturing a dressing according to claim 1, wherein the The fiber diameter of the cellulose is from 20 nm to 100 nm. 如申請專利範圍第1項所述之敷材的製造方法,更包括:進行一冷凍程序,其中該冷凍程序之溫度小於0℃且大於-14℃;以及進行一解凍程序,其中該解凍程序之時間為10分鐘至20分鐘。 The method of manufacturing a dressing according to claim 1, further comprising: performing a freezing process, wherein the temperature of the freezing process is less than 0 ° C and greater than -14 ° C; and performing a thawing procedure, wherein the thawing procedure The time is 10 minutes to 20 minutes.
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