[問題] 第一次看PAPER 請各位大大幫幫我
不知道在這裡可不可以問這些問題
這是我第一次讀paper 然後要報告
小弟程度真的不是很好
遇到很多問題
不知道有沒有大大可以幫我解答
感機不盡>"<
篇名是difution characterist of collagen film
<原文>Collagen films prepared by treating collagen gel
solutions with different concentrations of glutaraldehyde
were evaluated as a biodegradable and biocompatible
drug carrier for cosmetically effective agents in this
study.
在這個論文裡論述膠原蛋白膠體溶液再不同濃度的
戊二酸醛裡 討論藥物傳輸的生物降解性與生物相容
性(這一段是摘要的 cosmetically這個字真的就不知道
怎麼翻)
Then the gel solutions were put into a jacketed
container to measure the viscosity. A circulating water
bath was connected to this jacketed container for
maintaining the temperature of the container at 258C.
*jacketed container 是什麼樣的容器
*circulating water bath是什麼維持溫度的系統!?
水蒸氣嗎?
<原文> a suitable spindle was mounted and activated
with a desired rotating speed,and measurements
were taken after the designated temperature was
reached and a stable reading was recorded.
The viscosity was recorded at predetermined time
intervals. An average of three replicates was
reported for each time point.
*spindle這是什麼形狀
實驗步驟有點看不懂 是先把它轉成薄膜在量他的
黏度嗎?
<原文>A collagen solution at 1% (w/w) was prepared
by dissolving collagen in 3% acetic acid.
Then various concentrations of glutaraldehyde
(0, 0.05, 0.075, 0.1, 0.2, 0.25, and 0.3%, v/w)
were added, and these mixtures were immediately
transferred into a round acrylic mold, which had been
sealed with parafilm paper (American Can, USA) around
the bottom.These molds were then placed in an electric
dryer(Intech, Osaka, Japan) until the weight of the
collagen film approached a constant value.
Then, the parafilm paper was carefully peeled off,
and the collagen films were stored in a desiccator
at ambient temperature until use. The thickness of the
collagen films was measured at five different randomly
selected places. The uniformity of the thickness of
collagen films was acceptable since the coefficient
of variation was less than 5%.
round acrylic mold是類似培養皿的樣子嗎?
<翻譯>把膠原蛋白溶在3%的醋酸溶液裡配成1%的
膠原蛋白溶液 並加入(0 0.05 0.075 0.1 0.2 0.25 0.3v/w)
的戊二酸醛 並直接加入圓形丙烯酸的模子裡
並用石蠟紙密封 並放置在電子乾燥器裡 直到膠原蛋白膜的重量幾乎不變 在把時蠟紙小
心的撕掉 並把膠原蛋白儲藏在乾燥溫度的環境 將厚的膠原蛋白膜在隨機不同的地方量測
The uniformity of the thickness of collagen films was
acceptable since the coefficient of variation was less
than 5%.
這句就不大懂
<原文>
Diffusion studies were carried out using retinoic acid
(0.01%), retinol palmitate (0.1%), ascorbic acid
6-palmitate (0.1%), and tocopherol acetate (0.1%)
as model drugs either in solution or a gel form
(using1%, w/w, collagen as a gelling agent and 10%Cremophor RH40 as a solubilizer) at 378C, in a
flow-through diffusion system. This system
consists of a multi-channel peristaltic pump (202U/AA,
Watson Marlow), a fraction collector
(Retriever IV,ISCO, USA), a circulating water bath, and
six units of flow-through diffusion cells. The
flow-through diffusion cells contain two side arms,
which enable the conduction of receiver-cell media from
a peristaltic pump to a fraction collector. The temperature
was maintained at 378C by circulating constant
temperature water through the outer jacket of the
receiver cell. The surface area of the receiver cell
opening was 1.77 cm , and the volumes for the
donor and receiver compartments were 0.8 and 0.1ml,
respectively. A 0.9% normal saline solution
(containing 0.01% sodium azide and 10% Cremophor
RH40) was used as the receiver cell
medium. The receiver cell media were stirred at 450
rpm by externally driven, teflon-coated magnetic
bars. Collagen films prepared with different
concentrations of glutaraldehyde were mounted onto
each receiver cell, and an O-ring and cell top were
placed on the top of each membrane. These com-
ponents were then clamped securely in place.
The receiver cell medium reservoir was maintained at
378C. Subsequently, a solution or gel form of the
model drugs was applied on the top of each collagen
film. All samples were collected over 10-h periods.
The diffusion of model drugs through collagen films was
followed by determining their concentrations in the
collected medium as a function of time.
The concentrations of these model drugs were analyzed
by a validated HPLC method as described below.
1.multi-channel peristaltic pump (202U/AA,Watson
Marlow), a fraction collector (Retriever IV,ISCO, USA),
a circulating water bath (這些是怎樣的儀器!?)
2.因為很多儀器都沒有使用過 所以真的不懂他的
實驗流程 可能要麻煩大大解說一下 不用翻譯
大概說明一下他的實驗流程
好長一篇
怕沒有人回
很快就要報告了 真的需要大家幫我
也希望給我一些意見 對於以後做專題 還有讀paper
感謝各位大大
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