Zeng X M, Martin G P, Marriott C
Department of Pharmacy, King's College London, Franklin-Wilkins Building, 150 Stamford Street, SE1 8WA, London, UK.
Int J Pharm. 2001 May 7;218(1-2):63-73. doi: 10.1016/s0378-5173(01)00613-5.
The purpose of the present study was to investigate the effects of molecular weight (MW) of polyvinylpyrrolidone (PVP) on glass transition and crystallization of sucrose. Thus, sucrose was co-lyophilized with 2.5 and 5.0% w/w PVP of different molecular weights, which were characterized using gel permeation chromatography. Freeze drying was carried out for 48 h at a shelf temperature of -40 degrees C and a pressure of about 36 Pa. The samples were then dried in a vacuum oven at 24 degrees C for 12 h before drying for a further 12 h at 40 degrees C. Differential scanning calorimetry (DSC) was employed to measure the glass transition temperature (Tg), dynamic crystallization temperature (Tc) and isothermal crystallization induction time (tc) at 85 degrees C of sucrose. Isothermal water vapour sorption of each sample was also measured at different relative humidities. Tg values of sucrose varied from 48.3+/-0.8 degrees C for freeze-dried (FD) sucrose alone to 58.8+/-0.8 degrees C for the mixture containing 5.0% PVP of nominal MW 300 K. PVP increased sucrose T(g) significantly (ANOVA P<0.05). Although there was no significant difference (P>0.05) in Tg of the mixtures containing 2.5% w/w PVP of different MW, samples with 5.0% PVP of MW 300 K produced a significantly higher (P<0.05) Tg than the other mixtures. All mixtures were shown to possess higher (P<0.01) Tc than FD sucrose alone, which exhibited a T(c) of approximately 85 degrees C. PVP of MW 300 K consistently induced a significantly (P<0.05) higher Tc of sucrose than PVP of smaller MW. Increasing PVP concentration from 2.5 to 5.0% also resulted in a substantial increase in sucrose Tc. Using isothermal water vapour absorption, sucrose tc was found to increase up to over 10 times when it was co-lyophilized with 2.5% PVP, the actual value of tc being dependent upon the MW of the PVP. For example, PVP of MW 300 K resulted in a sucrose tc at 85 degrees C (89.1-95.6 min), which was approximately seven times higher than that of 2.5% PVP of MW 24 or 40 K. A longer tc of sucrose was also observed for mixtures containing PVP of MW 300 K than when sucrose was mixed with PVP of smaller MW. Thus the effect of PVP on sucrose Tg, Tc and tc was found to be dependent upon MW. PVP of higher MW was more efficient in inhibiting sucrose crystallization and by stabilizing glassy structures of the sugar, these polymers may improve the stability of co-lyophilized proteins and peptides.
本研究的目的是探究聚乙烯吡咯烷酮(PVP)的分子量(MW)对蔗糖玻璃化转变和结晶的影响。因此,将蔗糖与2.5%和5.0%(w/w)不同分子量的PVP进行共冻干,这些PVP通过凝胶渗透色谱进行表征。在搁板温度为-40℃、压力约为36 Pa的条件下进行48小时的冷冻干燥。然后将样品在24℃的真空烘箱中干燥12小时,接着在40℃下再干燥12小时。采用差示扫描量热法(DSC)测量蔗糖在85℃时的玻璃化转变温度(Tg)、动态结晶温度(Tc)和等温结晶诱导时间(tc)。还在不同相对湿度下测量了每个样品的等温水蒸气吸附情况。蔗糖的Tg值从单独冻干(FD)蔗糖的48.3±0.8℃变化到含有标称分子量为300 K的5.0% PVP的混合物的58.8±0.8℃。PVP显著提高了蔗糖的Tg(方差分析P<0.05)。尽管含有不同分子量2.5%(w/w)PVP的混合物的Tg没有显著差异(P>0.05),但分子量为300 K的5.0% PVP样品产生的Tg显著高于其他混合物(P<0.05)。所有混合物的Tc均高于单独的FD蔗糖(P<0.01),FD蔗糖的Tc约为85℃。分子量为300 K的PVP始终诱导蔗糖产生显著高于较小分子量PVP的Tc(P<0.05)。将PVP浓度从2.5%提高到5.0%也导致蔗糖Tc大幅增加。通过等温水蒸气吸收发现,当蔗糖与2.