中国医药导报
中國醫藥導報
중국의약도보
CHINA MEDICAL HERALD
2015年
23期
25-28
,共4页
刘铁楠%吴春涛%苏鹏宇%李素新%张志婓
劉鐵楠%吳春濤%囌鵬宇%李素新%張誌婓
류철남%오춘도%소붕우%리소신%장지비
雨生红球藻%虾青素%丙酮%提取%稳定性
雨生紅毬藻%蝦青素%丙酮%提取%穩定性
우생홍구조%하청소%병동%제취%은정성
Haematococcus pluvialis%Astaxanthin%Acetone%Extraction%Stability
目的:以雨生红球藻为原料,研究有机溶剂提取虾青素的条件及其稳定性。方法通过试验选取乙酸乙酯、丙酮、二氯甲烷、无水乙醇和二氯甲烷:丙酮(2:1)为提取溶剂,研究不同提取溶剂对虾青素提取效果的影响;应用试验得到的最佳溶剂分别于20、30、40、50、60、70、80℃下提取虾青素,确定最佳提取温度;在所得到的最适温度和溶剂下分别提取1、1.5、2、2.5、3 h确定最佳提取时间;设定提取次数分别为1、2、3次,提取后测定其OD480,研究提取次数对虾青素提取效果的影响;采用上述实验中优选出的提取溶剂、温度和时间,料液比分别取1:5、1:10、1:15、1:20、1:25,1:30、1:35、1:40,提取完成后测定其OD480,考察不同料液比对总虾青素提取率的影响。测定虾青素提取液在不同光照(自然光、日光、避光)、温度(30、40、50、60、70、80℃)、酸碱度(pH 8~14)等条件下的吸光度,以研究虾青素的稳定性。结果虾青素的提取中二次提取可获得90%虾青素,当料液比为1:25时所测吸光值最大;二氯甲烷:丙酮(2:1)为最佳提取液。随光照强度增加以及碱浓度增加,虾青素的降解增加。60℃以下,温度对虾青素的影响较小,60℃以上,虾青素开始受热破坏。结论二氯甲烷:丙酮(2:1)是最适的提取溶剂,1:25为最佳料液比;二次提取后已经提取出大部分虾青素,光照可导致虾青素的降解,虾青素对碱不稳定;虾青素在60℃以下比较稳定。
目的:以雨生紅毬藻為原料,研究有機溶劑提取蝦青素的條件及其穩定性。方法通過試驗選取乙痠乙酯、丙酮、二氯甲烷、無水乙醇和二氯甲烷:丙酮(2:1)為提取溶劑,研究不同提取溶劑對蝦青素提取效果的影響;應用試驗得到的最佳溶劑分彆于20、30、40、50、60、70、80℃下提取蝦青素,確定最佳提取溫度;在所得到的最適溫度和溶劑下分彆提取1、1.5、2、2.5、3 h確定最佳提取時間;設定提取次數分彆為1、2、3次,提取後測定其OD480,研究提取次數對蝦青素提取效果的影響;採用上述實驗中優選齣的提取溶劑、溫度和時間,料液比分彆取1:5、1:10、1:15、1:20、1:25,1:30、1:35、1:40,提取完成後測定其OD480,攷察不同料液比對總蝦青素提取率的影響。測定蝦青素提取液在不同光照(自然光、日光、避光)、溫度(30、40、50、60、70、80℃)、痠堿度(pH 8~14)等條件下的吸光度,以研究蝦青素的穩定性。結果蝦青素的提取中二次提取可穫得90%蝦青素,噹料液比為1:25時所測吸光值最大;二氯甲烷:丙酮(2:1)為最佳提取液。隨光照彊度增加以及堿濃度增加,蝦青素的降解增加。60℃以下,溫度對蝦青素的影響較小,60℃以上,蝦青素開始受熱破壞。結論二氯甲烷:丙酮(2:1)是最適的提取溶劑,1:25為最佳料液比;二次提取後已經提取齣大部分蝦青素,光照可導緻蝦青素的降解,蝦青素對堿不穩定;蝦青素在60℃以下比較穩定。
목적:이우생홍구조위원료,연구유궤용제제취하청소적조건급기은정성。방법통과시험선취을산을지、병동、이록갑완、무수을순화이록갑완:병동(2:1)위제취용제,연구불동제취용제대하청소제취효과적영향;응용시험득도적최가용제분별우20、30、40、50、60、70、80℃하제취하청소,학정최가제취온도;재소득도적최괄온도화용제하분별제취1、1.5、2、2.5、3 h학정최가제취시간;설정제취차수분별위1、2、3차,제취후측정기OD480,연구제취차수대하청소제취효과적영향;채용상술실험중우선출적제취용제、온도화시간,료액비분별취1:5、1:10、1:15、1:20、1:25,1:30、1:35、1:40,제취완성후측정기OD480,고찰불동료액비대총하청소제취솔적영향。측정하청소제취액재불동광조(자연광、일광、피광)、온도(30、40、50、60、70、80℃)、산감도(pH 8~14)등조건하적흡광도,이연구하청소적은정성。결과하청소적제취중이차제취가획득90%하청소,당료액비위1:25시소측흡광치최대;이록갑완:병동(2:1)위최가제취액。수광조강도증가이급감농도증가,하청소적강해증가。60℃이하,온도대하청소적영향교소,60℃이상,하청소개시수열파배。결론이록갑완:병동(2:1)시최괄적제취용제,1:25위최가료액비;이차제취후이경제취출대부분하청소,광조가도치하청소적강해,하청소대감불은정;하청소재60℃이하비교은정。
Objective To study the conditions and stability of astaxanthin extracted by organic solvent, taking Haema-tococcus pluvialis as raw materials. Methods The ethyl acetate, acetone, methylene chloride, absolute ethyl alcohol and methylene chloride : acetone (2:1) were selected as extraction solvent by experiments, the effect of different extraction solvents for extraction of astaxanthin was studied; the optimum solvent gained from the experiment was used to extract astaxanthin at 20, 30, 40, 50, 60, 70, 80℃, so as to determine the optimum extraction temperature; under the gained optimum temperature and solvent, the astaxanthin was extracted for 1, 1.5, 2, 2.5, 3 h respectively, so as to determine the optimum extraction time;the extraction times were set as 1, 2, 3 times, OD480 was measured after extraction, so as to study the effect of extraction times for extraction of astaxanthin; under the gained optimum solvent, temperature and time in the above experiments, the ratios of material to solvent were taken as 1:5, 1:10, 1:15, 1:20, 1:25, 1:30, 1:35, 1:40, OD480 was measured after extraction, so as to investigate the effect of different ratios of material to solvent for extraction of astaxanthin. The stability of astaxanthin was researched, and the absorbance of astaxanthin extracting solution was determined at different conditions of light (natural light, sunlight, lucifuge), temperature (30, 40, 50, 60, 70, 80℃), acid-base (pH 8-14), and so on. Results In the extraction of astaxanthin, the secondary extraction can obtain 90% of astaxanthin. When the ratio of material to solvent was 1:25, the measured absorbance was maximum. Methylene chlo-ride:acetone (2:1) was the best extracting solution. The degradation of astaxanthin increased with the increase of light in-tensity and the increase of alkali concentration. Below 60℃, the effect of temperature on astaxanthin was small. Above 60℃, astaxanthin began to be heated and damaged. Conclusion Methylene chloride : acetone (2:1) is best extracting solution, and 1:25 is the best ratio of material to solvent. the secondary extraction can extract most of astaxanthin, light can lead to degradation of astaxanthin, astaxanthin is unstable to alkali, astaxanthin is relatively stable below 60℃.