Article(id=1321425759038717991, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425717926154257, articleNumber=null, orderNo=null, doi=10.20251/j.cnki.1003-3734.2026.12.009, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=1762099200000, acceptedDateStr=2025-11-03, onlineDate=1792982051857, onlineDateStr=2026-10-26, pubDate=1782748800000, pubDateStr=2026-06-30, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792982051857, onlineIssueDateStr=2026-10-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792982051857, creator=13701087609, updateTime=1792982051857, updator=13701087609, issue=Issue{id=1321425717926154257, tenantId=1146029695717560320, journalId=1235980733773295621, year='2026', volume='35', issue='12', pageStart='1233', pageEnd='1344', issueExtLink='null', onlineDate='null', pubDate='1782748800000', pubDateStr='2026-06-30', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792982042056, creator='13701087609', updateTime=1792982988069, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1321429686186529703, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425717926154257, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1321429686186529704, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425717926154257, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1296, endPage=1303, ext={EN=ArticleExt(id=1321425759240044584, articleId=1321425759038717991, tenantId=1146029695717560320, journalId=1235980733773295621, language=EN, title=Study on glycerol doping to enhance the volatility-reducing effect of 4-n-hexadecyloxybenzaldehyde hydrazone xerogel on borneol, columnId=null, journalTitle=Chinese Journal of New Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective:

To prepare a borneol-low molecular organic gelator xerogel and evaluate its effect on borneol volatility.

Methods:

4-Hydroxybenzaldehyde was used as the starting material, and the target low molecular organic gelator was synthesized through Williamson etherification reaction and condensation reaction. The gel was prepared by dissolving borneol and low molecular organic gelator in anhydrous ethanol and subsequently undergoing vacuum freeze-drying to remove the solvent, resulting in the borneol-low molecular organic gelator xerogel. The microscopic morphology of the xerogel was observed by scanning electron microscope (SEM). The phase transition temperature was determined by differential scanning calorimeter (DSC). The driving force for the gel formation was analyzed by Fourier transform infrared spectroscopy (FT-IR). The loss of borneol from borneol sample, borneol-low molecular organic gelator xerogel, and the borneol-low molecular organic gelator-glycerol xerogel were compared by accelerated evaporation experiment over 10 h.

Results:

Mixtures of borneol and low molecular organic gelator with mass ratios of 2∶1, 3∶1 and 4∶1 formed a gel in anhydrous ethanol. SEM imaging revealed that the low molecular organic gelator showed a multilayered sheet-like structure. In contrast, the microstructures of the borneol-low molecular organic gelator xerogel with mass ratios of 2∶1, 3∶1 and 4∶1 showed a bulk, sheet-like and reticulate structure, respectively, which proved that the assemblies were formed. Furthermore, the addition of glycerol to the borneol-low molecular organic gelator system did not significantly alter the microstructure of the resulting xerogel. DSC analysis showed that the heat absorption peaks of the borneol-low molecular organic gelator xerogel varied with the mass ratios. FT-IR analysis revealed a shift in the hydroxyl group stretching vibration to lower wavenumbers for both borneol-low molecular organic gelator xerogel and borneol-low molecular organic gelator-glycerol xerogel, confirming that hydrogen bonding was involved in the formation of gel. After the 5 h accelerated volatilization test at 50 ℃, the borneol loss rate was 39.34% from borneol sample, while it was 17.40% from the 4∶1 borneol-low molecular organic gelator xerogel, and 9.98% after glycerol was added.

Conclusion:

The borneol-low molecular organic gelator xerogel reduces the volatility of borneol, with a further reduction observed upon the addition of glycerol.

, authors=Miao ZHANG1, 2, 3, 4, Bao-tong HAN1, 2, 3, 4, Nan JIA5, Dong-dong ZHANG1, 2, 3, 4, Wen-li HUANG1, 2, 3, 4, Yu-ze LI1, 2, 3, 4, Yun-dong XIE1, 2, 3, 4, Hua-wei ZHANG1, 2, 3, 4, Chong DENG1, 2, 3, 4, Xin-jie YANG1, Xiao-mei SONG1, 2, 3, 4, Yi JIANG1, 2, 3, 4, *, Hong XU1, 2, 3, 4, *, authorsList=Miao ZHANG, Bao-tong HAN, Nan JIA, Dong-dong ZHANG, Wen-li HUANG, Yu-ze LI, Yun-dong XIE, Hua-wei ZHANG, Chong DENG, Xin-jie YANG, Xiao-mei SONG, Yi JIANG, Hong XU, authorCompany=null, correspAuthors=Yi JIANG, Hong XU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1321425759600754729, articleId=1321425759038717991, tenantId=1146029695717560320, journalId=1235980733773295621, language=CN, title=甘油掺杂提高4-正十六烷氧基苯甲腙干凝胶降低冰片挥发性作用研究, columnId=1236330556003242277, journalTitle=中国新药杂志, columnName=实验研究, runingTitle=null, highlight=null, articleAbstract=
目的:

制备“冰片-小分子胶凝剂”干凝胶,评价其对冰片挥发性的影响。

方法:

以对羟基苯甲醛为起始化合物,经过Williamson醚化反应、缩合反应得到目标小分子胶凝剂;将冰片与小分子胶凝剂溶于无水乙醇,制备“冰片-小分子胶凝剂”凝胶,真空冷冻干燥后得到“冰片-小分子胶凝剂”干凝胶;利用扫描电子显微镜(scanning electron microscope, SEM)观察干凝胶微观形态,差示扫描量热仪(differential scanning calorimetry, DSC)测定干凝胶相变温度,傅里叶变换红外光谱(Fourier transform infrared spectroscopy, FT-IR)分析凝胶形成的驱动力;通过加速挥发实验对比冰片、“冰片-小分子胶凝剂”干凝胶、“冰片-小分子胶凝剂-甘油”干凝胶在10 h内冰片的挥发损失率。

结果:

“冰片-小分子胶凝剂”质量比2∶1、3∶1、4∶1时在无水乙醇中均形成凝胶;小分子胶凝剂SEM图为多层片状结构,“冰片-小分子胶凝剂”干凝胶质量比2∶1、3∶1、4∶1时的微观结构分别为块状、片状、网状结构,证明形成组装体;甘油加入“冰片-小分子胶凝剂”体系后形成干凝胶,其微观结构未发生显著改变。DSC中不同质量比“冰片-小分子胶凝剂”干凝胶吸热峰有相应变化;FT-IR中“冰片-小分子胶凝剂”干凝胶与“冰片-小分子胶凝剂-甘油”干凝胶中羟基伸缩振动峰向低波数移动,证实氢键参与凝胶形成。在50 ℃加速挥发实验中,冰片在5 h内损失率为39.34%,“冰片-小分子胶凝剂”干凝胶质量比4∶1时在5 h内冰片损失率为17.40%,添加甘油后,冰片损失率降低至9.98%。

结论:

“冰片-小分子胶凝剂”干凝胶可以降低冰片挥发性,且甘油的加入可进一步降低冰片挥发。

, authors=张苗1, 2, 3, 4, 韩宝彤1, 2, 3, 4, 贾楠5, 张东东1, 2, 3, 4, 黄文丽1, 2, 3, 4, 李玉泽1, 2, 3, 4, 谢允东1, 2, 3, 4, 张化为1, 2, 3, 4, 邓翀1, 2, 3, 4, 杨新杰1, 宋小妹1, 2, 3, 4, 姜祎1, 2, 3, 4, *, 徐虹1, 2, 3, 4, *, authorsList=张苗, 韩宝彤, 贾楠, 张东东, 黄文丽, 李玉泽, 谢允东, 张化为, 邓翀, 杨新杰, 宋小妹, 姜祎, 徐虹, authorCompany=null, correspAuthors=姜祎, 徐虹, authorNote=

张苗,女,硕士研究生,研究方向:中药提取分离分析技术与应用研究。E-mail: 。

, correspAuthorsNote=
* 姜祎,男,教授,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
* 徐虹,女,讲师,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
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2Shanxi Key Laboratory of Chinese Medicine Fundamentals and New Drugs Research, Shanxi University of Chinese Medicine, Xianyang 712046, China
3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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3陕西中医药大学 陕西省中医药管理局中药药效学与物质基础重点实验室,咸阳 712046
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张苗,女,硕士研究生,研究方向:中药提取分离分析技术与应用研究。E-mail: 。

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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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甘油掺杂提高4-正十六烷氧基苯甲腙干凝胶降低冰片挥发性作用研究
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张苗 1, 2, 3, 4 , 韩宝彤 1, 2, 3, 4 , 贾楠 5 , 张东东 1, 2, 3, 4 , 黄文丽 1, 2, 3, 4 , 李玉泽 1, 2, 3, 4 , 谢允东 1, 2, 3, 4 , 张化为 1, 2, 3, 4 , 邓翀 1, 2, 3, 4 , 杨新杰 1 , 宋小妹 1, 2, 3, 4 , 姜祎 1, 2, 3, 4, * , 徐虹 1, 2, 3, 4, *
中国新药杂志 | 实验研究 2026,35(12): 1296-1303
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中国新药杂志 |实验研究 2026 , 35 (12) : 1296 -1303
甘油掺杂提高4-正十六烷氧基苯甲腙干凝胶降低冰片挥发性作用研究
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张苗,女,硕士研究生,研究方向:中药提取分离分析技术与应用研究。E-mail: 。

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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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2陕西中医药大学 陕西省中药基础与新药研究重点实验室,咸阳 712046
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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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2陕西中医药大学 陕西省中药基础与新药研究重点实验室,咸阳 712046
3陕西中医药大学 陕西省中医药管理局中药药效学与物质基础重点实验室,咸阳 712046
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2Shanxi Key Laboratory of Chinese Medicine Fundamentals and New Drugs Research, Shanxi University of Chinese Medicine, Xianyang 712046, China
3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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2Shanxi Key Laboratory of Chinese Medicine Fundamentals and New Drugs Research, Shanxi University of Chinese Medicine, Xianyang 712046, China
3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
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2陕西中医药大学 陕西省中药基础与新药研究重点实验室,咸阳 712046
3陕西中医药大学 陕西省中医药管理局中药药效学与物质基础重点实验室,咸阳 712046
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张苗1, 2, 3, 4 , 韩宝彤1, 2, 3, 4, 贾楠5, 张东东1, 2, 3, 4, 黄文丽1, 2, 3, 4, 李玉泽1, 2, 3, 4, 谢允东1, 2, 3, 4, 张化为1, 2, 3, 4, 邓翀1, 2, 3, 4, 杨新杰1, 宋小妹1, 2, 3, 4, 姜祎1, 2, 3, 4, * , 徐虹1, 2, 3, 4, *
作者信息
  • 1陕西中医药大学 药学院,咸阳 712046
  • 2陕西中医药大学 陕西省中药基础与新药研究重点实验室,咸阳 712046
  • 3陕西中医药大学 陕西省中医药管理局中药药效学与物质基础重点实验室,咸阳 712046
  • 4陕西中医药大学陕西省中医药管理局太白七药研究与应用重点实验室,咸阳 712046
  • 5西安文理学院化学工程学院,西安 710000
通讯作者:
* 姜祎,男,教授,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
* 徐虹,女,讲师,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
作者简介:

张苗,女,硕士研究生,研究方向:中药提取分离分析技术与应用研究。E-mail: 。

Study on glycerol doping to enhance the volatility-reducing effect of 4-n-hexadecyloxybenzaldehyde hydrazone xerogel on borneol
Miao ZHANG1, 2, 3, 4 , Bao-tong HAN1, 2, 3, 4, Nan JIA5, Dong-dong ZHANG1, 2, 3, 4, Wen-li HUANG1, 2, 3, 4, Yu-ze LI1, 2, 3, 4, Yun-dong XIE1, 2, 3, 4, Hua-wei ZHANG1, 2, 3, 4, Chong DENG1, 2, 3, 4, Xin-jie YANG1, Xiao-mei SONG1, 2, 3, 4, Yi JIANG1, 2, 3, 4, * , Hong XU1, 2, 3, 4, *
Affiliations
  • 1College of Pharmacy, Shanxi University of Chinese Medicine, Xianyang 712046, China
  • 2Shanxi Key Laboratory of Chinese Medicine Fundamentals and New Drugs Research, Shanxi University of Chinese Medicine, Xianyang 712046, China
  • 3Key Laboratory of Pharmacodynamics and Material Basis of Chinese Medicine of Shanxi Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Xianyang 712046, China
  • 4Shanxi Key Laboratory of Research and Application of "Taibai Qiyao", Shanxi University of Chinese Medicine, Xianyang 712046, China
  • 5Xi'an University of Arts and Sciences, College of Chemical Engineering, Xi'an 710000, China
出版时间: 2026-06-30 doi: 10.20251/j.cnki.1003-3734.2026.12.009
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目的:

制备“冰片-小分子胶凝剂”干凝胶,评价其对冰片挥发性的影响。

方法:

以对羟基苯甲醛为起始化合物,经过Williamson醚化反应、缩合反应得到目标小分子胶凝剂;将冰片与小分子胶凝剂溶于无水乙醇,制备“冰片-小分子胶凝剂”凝胶,真空冷冻干燥后得到“冰片-小分子胶凝剂”干凝胶;利用扫描电子显微镜(scanning electron microscope, SEM)观察干凝胶微观形态,差示扫描量热仪(differential scanning calorimetry, DSC)测定干凝胶相变温度,傅里叶变换红外光谱(Fourier transform infrared spectroscopy, FT-IR)分析凝胶形成的驱动力;通过加速挥发实验对比冰片、“冰片-小分子胶凝剂”干凝胶、“冰片-小分子胶凝剂-甘油”干凝胶在10 h内冰片的挥发损失率。

结果:

“冰片-小分子胶凝剂”质量比2∶1、3∶1、4∶1时在无水乙醇中均形成凝胶;小分子胶凝剂SEM图为多层片状结构,“冰片-小分子胶凝剂”干凝胶质量比2∶1、3∶1、4∶1时的微观结构分别为块状、片状、网状结构,证明形成组装体;甘油加入“冰片-小分子胶凝剂”体系后形成干凝胶,其微观结构未发生显著改变。DSC中不同质量比“冰片-小分子胶凝剂”干凝胶吸热峰有相应变化;FT-IR中“冰片-小分子胶凝剂”干凝胶与“冰片-小分子胶凝剂-甘油”干凝胶中羟基伸缩振动峰向低波数移动,证实氢键参与凝胶形成。在50 ℃加速挥发实验中,冰片在5 h内损失率为39.34%,“冰片-小分子胶凝剂”干凝胶质量比4∶1时在5 h内冰片损失率为17.40%,添加甘油后,冰片损失率降低至9.98%。

结论:

“冰片-小分子胶凝剂”干凝胶可以降低冰片挥发性,且甘油的加入可进一步降低冰片挥发。

小分子胶凝剂  /  冰片  /  自组装  /  挥发性  /  甘油掺杂
Objective:

To prepare a borneol-low molecular organic gelator xerogel and evaluate its effect on borneol volatility.

Methods:

4-Hydroxybenzaldehyde was used as the starting material, and the target low molecular organic gelator was synthesized through Williamson etherification reaction and condensation reaction. The gel was prepared by dissolving borneol and low molecular organic gelator in anhydrous ethanol and subsequently undergoing vacuum freeze-drying to remove the solvent, resulting in the borneol-low molecular organic gelator xerogel. The microscopic morphology of the xerogel was observed by scanning electron microscope (SEM). The phase transition temperature was determined by differential scanning calorimeter (DSC). The driving force for the gel formation was analyzed by Fourier transform infrared spectroscopy (FT-IR). The loss of borneol from borneol sample, borneol-low molecular organic gelator xerogel, and the borneol-low molecular organic gelator-glycerol xerogel were compared by accelerated evaporation experiment over 10 h.

Results:

Mixtures of borneol and low molecular organic gelator with mass ratios of 2∶1, 3∶1 and 4∶1 formed a gel in anhydrous ethanol. SEM imaging revealed that the low molecular organic gelator showed a multilayered sheet-like structure. In contrast, the microstructures of the borneol-low molecular organic gelator xerogel with mass ratios of 2∶1, 3∶1 and 4∶1 showed a bulk, sheet-like and reticulate structure, respectively, which proved that the assemblies were formed. Furthermore, the addition of glycerol to the borneol-low molecular organic gelator system did not significantly alter the microstructure of the resulting xerogel. DSC analysis showed that the heat absorption peaks of the borneol-low molecular organic gelator xerogel varied with the mass ratios. FT-IR analysis revealed a shift in the hydroxyl group stretching vibration to lower wavenumbers for both borneol-low molecular organic gelator xerogel and borneol-low molecular organic gelator-glycerol xerogel, confirming that hydrogen bonding was involved in the formation of gel. After the 5 h accelerated volatilization test at 50 ℃, the borneol loss rate was 39.34% from borneol sample, while it was 17.40% from the 4∶1 borneol-low molecular organic gelator xerogel, and 9.98% after glycerol was added.

Conclusion:

The borneol-low molecular organic gelator xerogel reduces the volatility of borneol, with a further reduction observed upon the addition of glycerol.

low molecular organic gelators  /  borneol  /  self-assembly  /  volatility  /  glycerol doping
张苗, 韩宝彤, 贾楠, 张东东, 黄文丽, 李玉泽, 谢允东, 张化为, 邓翀, 杨新杰, 宋小妹, 姜祎, 徐虹. 甘油掺杂提高4-正十六烷氧基苯甲腙干凝胶降低冰片挥发性作用研究. 中国新药杂志, 2026 , 35 (12) : 1296 -1303 . DOI: 10.20251/j.cnki.1003-3734.2026.12.009
Miao ZHANG, Bao-tong HAN, Nan JIA, Dong-dong ZHANG, Wen-li HUANG, Yu-ze LI, Yun-dong XIE, Hua-wei ZHANG, Chong DENG, Xin-jie YANG, Xiao-mei SONG, Yi JIANG, Hong XU. Study on glycerol doping to enhance the volatility-reducing effect of 4-n-hexadecyloxybenzaldehyde hydrazone xerogel on borneol[J]. Chinese Journal of New Drugs, 2026 , 35 (12) : 1296 -1303 . DOI: 10.20251/j.cnki.1003-3734.2026.12.009
  • 国家中医药管理局高水平中医药重点学科建设项目(304-174010324025)
  • 陕西中医药大学校级项目(604200002/303)
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doi: 10.20251/j.cnki.1003-3734.2026.12.009
  • 首发时间:2026-10-26
  • 出版时间:2026-06-30
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  • 录用日期:2025-11-03
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国家中医药管理局高水平中医药重点学科建设项目(304-174010324025)
陕西中医药大学校级项目(604200002/303)
作者信息
    1陕西中医药大学 药学院,咸阳 712046
    2陕西中医药大学 陕西省中药基础与新药研究重点实验室,咸阳 712046
    3陕西中医药大学 陕西省中医药管理局中药药效学与物质基础重点实验室,咸阳 712046
    4陕西中医药大学陕西省中医药管理局太白七药研究与应用重点实验室,咸阳 712046
    5西安文理学院化学工程学院,西安 710000

通讯作者:

* 姜祎,男,教授,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
* 徐虹,女,讲师,研究方向:中药药效物质基础及小分子凝胶研究。E-mail: 。
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