Chem. J. Chinese Universities ›› 2022, Vol. 43 ›› Issue (4): 20210860.doi: 10.7503/cjcu20210860
• Physical Chemistry • Previous Articles Next Articles
LI Lei1,2, FANG Yun2(), XIA Yongmei1(
), BO Chunling2, FAN Ye2
Received:
2021-12-27
Online:
2022-04-10
Published:
2022-02-16
Contact:
FANG Yun,XIA Yongmei
E-mail:yunfang@126.com;ymxia@jiangnan.edu.cn
Supported by:
CLC Number:
TrendMD:
LI Lei, FANG Yun, XIA Yongmei, BO Chunling, FAN Ye. Comparative Effects of Mono/disaccharides on Conjugated Linoleic Acid Vesicles at Near Neutral pH[J]. Chem. J. Chinese Universities, 2022, 43(4): 20210860.
Suspension | n(Saccharide)/n(CLA) | pH window | Average particle size/nm | Thermodynamic parameter/(kJ?mol-1) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
TEM | DLS | pH | ΔH | TΔS | ΔG | |||||
CLA | 0 | 7.8—9.2 | ― | ― | ― | ― | ― | ― | ||
L?CLA | 0.1∶1.0 | 7.3—9.4 | 20.6 | 22.5 | 7 | -0.55 | 11.40 | -11.95 | ||
0.5∶1.0 | 7.3—9.3 | 8 | -1.14 | 8.64 | -9.78 | |||||
1.0∶1.0 | 7.7—9.5 | 9 | -0.32 | 11.22 | -11.54 | |||||
T?CLA | 0.1∶1.0 | 7.3—9.3 | 20.4 | 22.6 | 7 | -0.12 | 21.83 | -21.95 | ||
0.5∶1.0 | 7.4—9.5 | |||||||||
1.0∶1.0 | 7.6—9.4 | |||||||||
S?CLA | 0.1∶1.0 | 7.2—9.3 | 21.3 | 23.6 | 7 | -0.90 | 9.75 | -10.65 | ||
0.5∶1.0 | 7.3—9.3 | |||||||||
1.0∶1.0 | 7.4—9.4 | |||||||||
R?CLA[ | 0.1∶1.0 | 7.0—9.5 | 22.5 | 26.4 | 7 | -5.08 | 10.54 | -15.63 |
Table 1 pH window for FAV formation, average particle size at the near neutral-side pH window, and thermodynamic parameter of disaccharide(or monosaccharide)-CLA suspensions
Suspension | n(Saccharide)/n(CLA) | pH window | Average particle size/nm | Thermodynamic parameter/(kJ?mol-1) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
TEM | DLS | pH | ΔH | TΔS | ΔG | |||||
CLA | 0 | 7.8—9.2 | ― | ― | ― | ― | ― | ― | ||
L?CLA | 0.1∶1.0 | 7.3—9.4 | 20.6 | 22.5 | 7 | -0.55 | 11.40 | -11.95 | ||
0.5∶1.0 | 7.3—9.3 | 8 | -1.14 | 8.64 | -9.78 | |||||
1.0∶1.0 | 7.7—9.5 | 9 | -0.32 | 11.22 | -11.54 | |||||
T?CLA | 0.1∶1.0 | 7.3—9.3 | 20.4 | 22.6 | 7 | -0.12 | 21.83 | -21.95 | ||
0.5∶1.0 | 7.4—9.5 | |||||||||
1.0∶1.0 | 7.6—9.4 | |||||||||
S?CLA | 0.1∶1.0 | 7.2—9.3 | 21.3 | 23.6 | 7 | -0.90 | 9.75 | -10.65 | ||
0.5∶1.0 | 7.3—9.3 | |||||||||
1.0∶1.0 | 7.4—9.4 | |||||||||
R?CLA[ | 0.1∶1.0 | 7.0—9.5 | 22.5 | 26.4 | 7 | -5.08 | 10.54 | -15.63 |
Suspension | n(Saccharide)/n(CLA) | pH window | Average particle size/nm | Thermodynamic parameter/(kJ?mol-1) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
TEM | DLS | pH | ΔH | TΔS | ΔG | |||||
L/R?CLA | 0.1∶0.1∶1.0 | 7.1—9.3 | 20.4 | 22.4 | 7 | -1.13 | 27.94 | -29.07 | ||
T/R?CLA | 0.1∶0.1∶1.0 | 6.9—9.3 | 22.5 | 24.0 | 7 | -1.05 | 27.57 | -28.62 | ||
S/R?CLA | 0.1∶0.1∶1.0 | 6.9—9.4 | 23.5 | 26.4 | 7 | -1.88 | 26.69 | -28.57 | ||
A/R?CLA | 0.1∶ 0.1∶1.0 | 6.5—9.2 | 18.3 | 20.7 | 7 | 2.85 | 31.26 | -28.41 | ||
G/R?CLA | 0.1∶0.1∶1.0 | 7.0—9.3 | 18.2 | 21.2 | 7 | -2.71 | 28.44 | -31.15 |
Table 2 pH window for CLA-FAV formation, average particle size at the near neutral-side pH window and thermodynamic parameter of disaccharide/R(or monosaccharide/R)-CLA suspensions
Suspension | n(Saccharide)/n(CLA) | pH window | Average particle size/nm | Thermodynamic parameter/(kJ?mol-1) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
TEM | DLS | pH | ΔH | TΔS | ΔG | |||||
L/R?CLA | 0.1∶0.1∶1.0 | 7.1—9.3 | 20.4 | 22.4 | 7 | -1.13 | 27.94 | -29.07 | ||
T/R?CLA | 0.1∶0.1∶1.0 | 6.9—9.3 | 22.5 | 24.0 | 7 | -1.05 | 27.57 | -28.62 | ||
S/R?CLA | 0.1∶0.1∶1.0 | 6.9—9.4 | 23.5 | 26.4 | 7 | -1.88 | 26.69 | -28.57 | ||
A/R?CLA | 0.1∶ 0.1∶1.0 | 6.5—9.2 | 18.3 | 20.7 | 7 | 2.85 | 31.26 | -28.41 | ||
G/R?CLA | 0.1∶0.1∶1.0 | 7.0—9.3 | 18.2 | 21.2 | 7 | -2.71 | 28.44 | -31.15 |
Solutions | n(Saccharide)/ n(CLA) | R(%) (no NaCl) | R(%) (0.2 mol/L NaCl) | Solutions | n(Saccharide)/ n(CLA) | R(%) (no NaCl) | R(%) (0.2 mol/L NaCl) |
---|---|---|---|---|---|---|---|
L?CLA | 0.1∶1.0 | 19.86±0.74 | 24.87±0.45 | S?CLA | 0.5∶1.0 | 10.51±1.26 | 19.37±0.45 |
0.5∶1.0 | 17.90±1.04 | 24.71±0.60 | 1.0∶1.0 | 10.14±2.99 | 16.97±1.30 | ||
1.0∶1.0 | 17.21±0.90 | 26.50±0.95 | L/R?CLA | 0.1∶0.1∶1.0 | 21.21±1.44 | 16.85±0.51 | |
T?CLA | 0.1∶1.0 | 16.81±0.56 | 17.16±1.13 | T/R?CLA | 0.1∶0.1∶1.0 | 17.28±0.99 | 16.70±0.56 |
0.5∶1.0 | 12.14±1.26 | 17.29±0.49 | S/R?CLA | 0.1∶0.1∶1.0 | 10.87±1.88 | 17.87±1.70 | |
1.0∶1.0 | 14.19±1.13 | 20.48±1.00 | A/R?CLA | 0.1∶0.1∶1.0 | 19.08±0.62 | 16.48±1.42 | |
S?CLA | 0.1∶1.0 | 8.15±1.44 | 17.87±1.88 | G/R?CLA | 0.1∶0.1∶1.0 | 20.64±1.28 | 16.78±0.89 |
Table 3 Values of R(%) influenced by disaccharide-CLA, disaccharide/R(or monosaccharide/R)-CLA suspensions
Solutions | n(Saccharide)/ n(CLA) | R(%) (no NaCl) | R(%) (0.2 mol/L NaCl) | Solutions | n(Saccharide)/ n(CLA) | R(%) (no NaCl) | R(%) (0.2 mol/L NaCl) |
---|---|---|---|---|---|---|---|
L?CLA | 0.1∶1.0 | 19.86±0.74 | 24.87±0.45 | S?CLA | 0.5∶1.0 | 10.51±1.26 | 19.37±0.45 |
0.5∶1.0 | 17.90±1.04 | 24.71±0.60 | 1.0∶1.0 | 10.14±2.99 | 16.97±1.30 | ||
1.0∶1.0 | 17.21±0.90 | 26.50±0.95 | L/R?CLA | 0.1∶0.1∶1.0 | 21.21±1.44 | 16.85±0.51 | |
T?CLA | 0.1∶1.0 | 16.81±0.56 | 17.16±1.13 | T/R?CLA | 0.1∶0.1∶1.0 | 17.28±0.99 | 16.70±0.56 |
0.5∶1.0 | 12.14±1.26 | 17.29±0.49 | S/R?CLA | 0.1∶0.1∶1.0 | 10.87±1.88 | 17.87±1.70 | |
1.0∶1.0 | 14.19±1.13 | 20.48±1.00 | A/R?CLA | 0.1∶0.1∶1.0 | 19.08±0.62 | 16.48±1.42 | |
S?CLA | 0.1∶1.0 | 8.15±1.44 | 17.87±1.88 | G/R?CLA | 0.1∶0.1∶1.0 | 20.64±1.28 | 16.78±0.89 |
1 | Morigaki K., Walde P., Curr. Opin. Colloid Interface Sci., 2007, 12(2), 75—80 |
2 | Guo X. N., Yang J. S., Polym. Int., 2021, 70(11), 1604—1611 |
3 | Fan Y., Liu T. T., Fang Y., Xia Y. M., Chem. J. Chinese Universities, 2019, 40(6), 1193—1200 |
樊晔, 刘婷婷, 方云, 夏咏梅. 高等学校化学学报, 2019, 40(6), 1193—1200 | |
4 | Szostak J. W., Angew. Chem. Int. Ed., 2017, 56(37), 11037—11043 |
5 | Martin N., Douliez J. P., ChemSystemsChem, 2021, 3, e2100024 |
6 | Gao J., Huang K. K., Zhang X. L., Sun Y., Feng S. H., Chem. J. Chinese Universities, 2018, 39(5), 849—854 |
高静, 黄科科, 张显龙, 孙宇, 冯守华. 高等学校化学学报, 2018, 39(5), 849—854 | |
7 | Garenne D., Beven L., Navailles L., Nallet F., Dufourc E. J., Douliez J. P., Angew. Chem. Int. Ed., 2016, 55(43), 13475—13479 |
8 | Fan Y., Cao C. M., Fang Y., Xia Y. M., Acta Phys. Chim Sin., 2022, 38(3), 2002032 |
樊晔, 曹崇梅, 方云, 夏咏梅. 物理化学学报, 2022, 38(3), 2002032 | |
9 | Cristiano M. C., Mancuso A., Fresta M., Torella D., de Gaetano F., Ventura C. A., Paolino D., Pharmaceutics, 2021, 13(4), 548—562 |
10 | Shen J., Wang Y. X., Fan P. P., Jiang L., Zhuang W., Han Y. W., Zhang H. M., Colloids Surf. A, 2019, 568, 66—74 |
11 | Ikari K., Sakuma Y., Jimbo T., Kodama A., Imai M., Monnard P. A., Rasmussen S., Soft Matter., 2015, 11(31), 6327—6334 |
12 | Fan Y., Fan M. Q., Fang Y., Li L., Pan H. Y., Xia Y. M., Chem. J. Chinese Universities, 2021, 42(8), 2574—2580 |
樊晔, 范梦琦, 方云, 李磊, 潘红阳, 夏咏梅. 高等学校化学学报, 2021, 42(8), 2574—2580 | |
13 | Zhou C. C., Cheng X. H., Zhao O. D., Liu S., Liu C. J., Wang J. D., Huang J. B., Soft Matter, 2014, 10(40), 8023—8030 |
14 | Black R. A., Blosser M. C., Stottrup B. L., Tavakley R., Deamer D. W., Keller S. L., Proc. Natl. Acad. Sci. U. S. A., 2013, 110(33), 13272—13276 |
15 | Black R. A., Blosser M. C., Life, 2016, 6(3), 33—47 |
16 | Cornell C. E., Black R. A., Xue M. J., Litz H. E., Ramsay A., Gordon M., Mileant A., Cohen Z. R., Williams J. A., Lee K. K., Drobny G. P., Keller S. L., Proc. Natl. Acad. Sci. U. S. A., 2019, 116(35), 17239—17244 |
17 | Xue M. J., Black R. A., Cornell C. E., Drobny G. P., Keller S. L., ChemBioChem, 2020, 21(19), 2764—2767 |
18 | Xue M. J., Black R. A., Cohen Z. R., Roehrich A., Drobny G. P., Keller S. L., J. Phys. Chem. B, 2021, 125(29), 7933—7939 |
19 | Visentini F. F., Perez A. A., Santiago L. G., Food Hydrocoll., 2019, 93, 242—252 |
20 | Dai J. N., Fan Y., Fang Y., Chem. J. Chinese Universities, 2015, 36(6), 1140—1145 |
戴基宁, 樊晔, 方云. 高等学校化学学报, 2015, 36(6), 1140—1145 | |
21 | Fan Y., Fang Y., Ma L., Colloids Surf. B, 2014, 123, 8—14 |
22 | Frisch M. J., Trucks G. W., Schlegel H. B., Scuseria G. E., Robb M. A., Cheeseman J. R., Scalmani G., Barone V., Petersson G. A., Nakatsuji H., Li X., Caricato M., Marenich A. V., Bloino J., Janesko B. G., Gomperts R., Mennucci B., Hratchian H. P., Ortiz J. V., Izmaylov A. F., Sonnenberg J. L., Williams-Young D., Ding F., Lipparini F., Egidi F., Goings J., Peng B., Petrone A., Henderson T., Ranasinghe D., Zakrzewski V. G., Gao J., Rega N., Zheng G., Liang W., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Vreven T., Throssell K., Montgomery J. A. Jr., Peralta J. E., Ogliaro F., Bearpark M. J., Heyd J. J., Brothers E. N., Kudin K. N., Staroverov V. N., Keith T. A., Kobayashi R., Normand J., Raghavachari K., Rendell A. P., Burant J. C., Iyengar S. S., Tomasi J., Cossi M., Millam J. M., Klene M., Adamo C., Cammi R., Ochterski J. W., Martin R. L., Morokuma K., Farkas O., Foresman J. B., Fox D. J., Gaussian 16, Revision C.01, Gaussian, Inc., Wallingford CT, 2016 |
23 | Li L., Fang Y., Xia Y. M., Bo C. L., Fan Y., J. Mol. Liq., 2022, 351, 118656 |
24 | Fan Y., Ma J., Fang Y., Liu T. T., Hu X. Y., Xia Y. M., Colloids Surf. B, 2018, 167, 385—391 |
25 | Goel K., Zuñiga⁃Bustos M., Lazurko C., Jacques E., Galaz⁃Araya C., Valenzuela⁃Henriquez F., Pacioni N. L., Couture J. F., Poblete H., Alarcon E. I., ACS Appl. Mater. Inter., 2019, 11(19), 17697—17705 |
26 | Wan Z. L., Wang L. Y., Yang X. Q., Wang J. M., Wang L. J., Food Hydrocoll., 2016, 52, 317—328 |
27 | Hu Y., Li H. L., Meng P. J., Li K. X., Xiong Y. M., Zhang S. H., Yang Y., Yin A. H., Huang P. L., Colloids Surf. B, 2020, 189, 110881 |
28 | Deamer D. W., Dworkin J. P., Chemistry and Physics of Primitive Membranes. In Prebiotic Chemistry: from Simple Amphiphiles to Protocell Models, Ed.: Walde P., Springer, Berlin, 2005, 259, 1—27 |
29 | Masjedi M., Montahaei T., J. Drug Deliv. Sci. Tec., 2021, 61, 102234 |
30 | Steed J. W., Atwood J. L., Supramolecular Chemistry, Wliley, Chichester, 2009, 27—29 |
[1] | LI Lei, FANG Yun, XIA Yongmei, FAN Mengqi, FAN Ye. Effects of Amine Structures on the pH Window of Oleic Acid Vesicle [J]. Chem. J. Chinese Universities, 2022, 43(8): 20220144. |
[2] | WANG Hong, SAN Khin Nyein Ei, FANG Yun, ZHANG Xinyu, FAN Ye. Pickering Emulsion Stabilization and Interfacial Catalytic Oxidation by Janus Nano-Au [J]. Chem. J. Chinese Universities, 2022, 43(6): 20220105. |
[3] | FAN Ye, FAN Mengqi, FANG Yun, LI Lei, PAN Hongyang, XIA Yongmei. Size Polydispersity of Oleic Acid Vesicles and Effects of Diols on the pH Window of the Vesicles [J]. Chem. J. Chinese Universities, 2021, 42(8): 2574. |
[4] | FAN Ye, LI Qian, FANG Yun, XIA Yongmei. Fabrication of Lamellar Liquid Crystals of Conjugated Linoleic Acid as Drug Delivery Systems † [J]. Chem. J. Chinese Universities, 2020, 41(4): 750. |
[5] | ZHANG Xinyu, WANG Hong, FANG Yun, FAN Ye. Stimuli-responsive Fe3O4 Nanoparticle Modified by Conjugated Linoleic Acid [J]. Chem. J. Chinese Universities, 2020, 41(11): 2519. |
[6] | FAN Ye,LIU Tingting,FANG Yun,XIA Yongmei. Vesiculation and Stability: Oligomer of Conjugated Linoleate Acids Prepared by High Internal Phase Self-emulsion Polymerization† [J]. Chem. J. Chinese Universities, 2019, 40(6): 1193. |
[7] | FAN Ye, ZHENG Yizhou, FANG Yun, XIA Yongmei, GAO Di, WANG Jie. Vesiculation of Sodium Conjugated Linoleate in Alkaline Conditions Induced by Oligomerization† [J]. Chem. J. Chinese Universities, 2018, 39(7): 1483. |
[8] | LIANG Xiaodan, FAN Ye, FANG Yun, XIA Yongmei, CHENG Ruohui. Investigation of Vesiculation of Conjugated Linoleic Acid Assisted by Monolauryl Phosphate† [J]. Chem. J. Chinese Universities, 2017, 38(9): 1639. |
[9] | DAI Jining, FAN Ye, FANG Yun. Temperature-responsive Expansion of Self-crosslinked Ufasomes of Conjugated Linoleic Acid† [J]. Chem. J. Chinese Universities, 2015, 36(6): 1140. |
[10] | FAN Ye, FANG Yun, CHEN Hanting, GAO Di. Preparation, SERS and Catalytic Properties of Au Nano-network Based on Poly(conjugated linoleic acid)† [J]. Chem. J. Chinese Universities, 2014, 35(9): 1933. |
[11] | FAN Ye, FANG Yun, GAO Di. Construction and Characterization of a Novel pH-insensitive Self-crosslinked Ufasome of Conjugated Linoleic Acid† [J]. Chem. J. Chinese Universities, 2014, 35(8): 1746. |
[12] | YAO Yan-Ping1,2, ZHU Zhen-Yuan2, XU Tong1, ZHANG Yong-Min2,3. Chemical Synthesis of N-Acetylchitooligosaccharide Analogues [J]. Chem. J. Chinese Universities, 2007, 28(2): 265. |
[13] | WU Shi, TENG Qi-Wen, CHEN Xiao-Fei, ZHOU Rong-Hui . Molecular Recognition and "on-off" Switching of Calix[4]arenes to Monosaccharides and Pyrimidine Derivatives [J]. Chem. J. Chinese Universities, 2003, 24(7): 1271. |
[14] | ZHANG Nian-Xiang, CAO Shu-Gui, DONG Huan, LIU Yan-Bin, REN Yi-Qing, HAN Si-Ping, YANG Hong. Studies on Synthesis of Monosaccharide Esters Catalyzed by Lipases in Organic Solvents [J]. Chem. J. Chinese Universities, 1996, 17(9): 1404. |
[15] | REN Ji-Cun, HE Jin-Lan, DENG Yan-Zhuo, CHENG Jie-Ke . Rapid Separation of Disaccharides by Capillary Zone Electrophoresis with Interference Refractive Index Detection [J]. Chem. J. Chinese Universities, 1993, 14(12): 1661. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||