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烟酰胺及其复配体系的稳定性研究 被引量:2

Study on the stability of niacinamide and its mixed system
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摘要 以5%烟酰胺、5%烟酰胺+0.5%MSH、5%烟酰胺+1.0%MSH 3个体系为研究对象,以高效液相色谱法测定烟酰胺水解产生烟酸的含量为指标,考察pH值、温度以及光照等条件对体系稳定性的影响。结果表明,各考察条件对体系的影响顺序依次为45℃>循环(-15℃~48℃)≈37℃光照>5℃≈-10℃;pH值对烟酰胺水解有显著的影响,特别是高温条件下,且pH值越大影响越显著;MSH会促进烟酰胺水解,且随着MSH含量增加影响程度增加,同时,pH值越大,MSH对体系的影响越大,但MSH对体系的影响小于pH值。因此,无论是在烟酰胺体系还是在烟酰胺与MSH复配体系,都应严格控制体系的pH值在6.0左右,尽量不要超过6.5,且应保持低温及避免光照。 The effects of pH,temperature and light on the stability of 5%niacinamide,5%niacinamide+0.5%MSH,5%niacinamide+1.0%MSH were studied by HPLC to detect the hydrolysis product nicotinic acid.The results show that the influences of conditions on the systems are in the decreasing order:45℃>cycle(-15℃~48℃)≈37℃lighting>5℃≈-10℃.pH has significant effects on the hydrolysis of niacinamide,especially at high temperatures(The higher the pH is,the more significant the effect will be).MSH can promote the hydrolysis of niacinamide,and such influence will increase with the increase of MSH content.Moreover,such influence of MSH will be higher at higher pH values.However,the influence of MSH on the systems is less than that of pH.Therefore,in the niacinamide system or the niacinamide/MSH mixed system,to inhibit the hydrolysis of niacinamide,the pH value should be controlled at approximately 6.0 and not exceeding 6.5,and the system should be kept at low temperature and avoid light.
作者 陈贞明 CHEN Zhen-ming(Fujian Pientzehuang Cosmetics Co.,Ltd.,Zhangzhou,Fujian 363000,China)
出处 《日用化学品科学》 CAS 2022年第5期29-35,共7页 Detergent & Cosmetics
关键词 烟酰胺 MSH 稳定性 PH值 niacinamide MSH stability pH
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  • 1Altschul R,Hoffer A,Stephen JD.Influence of nicotinic acid onserum cholesterol in man[J].Arch Biochem Biophys,1955,54(2):558-559.
  • 2Vaccari CS,Hammoud RA,Nagamia SH,Ramasamy K,DollarAL,Khan BV.Revisiting niacin:reviewing the evidence[J].JClin Lipidol,2007,1(4):248-255.
  • 3Tunaru S,Kero J,Schaub A,Wufka C,Blaukat A,Pfeffer K,et al.PUMA-G and HM74 are receptors for nicotinic acid andmediate its anti-lipolytic effect[J].Nat Med,2003,9(3):352-355.
  • 4Soga T,Kamohara M,Takasaki J,Matsumoto S,Saito T,Ohishi T,et al.Molecular identification of nicotinic acid receptor[J].BiochemBiophys Res Commun,2003,303(1):364-369.
  • 5Wise A,Foord SM,Fraser NJ,Barnes AA,Elshourbagy N,Eilert M,et al.Molecular identification of high and low affinityreceptors for nicotinic acid[J].J Biol Chem,2003,278(11):9869-9874.
  • 6Zellner C,Pullinger CR,Aouizerat BE,Frost PH,Kwok PY,Malloy MJ,et al.Variations in human HM74(GPR109B)andHM74A(GPR109A)niacin receptors[J].Hum Mutat,2005,25(1):18-21.
  • 7Maciejewski-Lenoir D,Richman JG,Hakak Y,Gaidarov I,Behan DP,Connolly DT.Langerhans cells release prostaglandinD2 in response to nicotinic acid[J].J Invest Dermatol,2006,126(12):2637-2646.
  • 8Taggart AK,Kero J,Gan X,Cai TQ,Cheng K,Ippolito M,et al.(D)-Beta-hydroxybutyrate inhibits adipocyte lipolysis viathe nicotinic acid receptor PUMA-G[J].J Biol Chem,2005,280(29):26649-26652.
  • 9Carlson LA,Oro L.The effect of nicotinic acid on the plasma freefatty acid;demonstration of a metabolic type of sympathicolysis[J].Acta Med Scand,1962,172:641-645.
  • 10Carlson LA.Studies on the effect of nicotinic acid on cate-cholamine stimulated lipolysis in adipose tissue in vitro[J].ActaMed Scand,1963,173:719-722.

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