Collect. Czech. Chem. Commun.
2005, 70, 269-291
https://doi.org/10.1135/cccc20050269
Recent Advances in Chemistry and Applications of Substituted Poly(ethylene glycol)s
Miloš Sedlák
Department of Organic Chemistry, Faculty of Chemical Technology, University of Pardubice, nám.Čs. legií 565, 532 10 Pardubice, Czech Republic
References
1a. Eur. J. Pharm. Sci. 2003, 20, 1.
< J.: https://doi.org/10.1016/S0928-0987(03)00164-7>
1b. J. Gene Med. 2004, 6, 597.
< M. L., Abedi M. R., Wixon J., Edelstein R. M.: https://doi.org/10.1002/jgm.619>
1c. Pharm. Res. 2005, 22, 1.
< M., Kim S. W.: https://doi.org/10.1007/s11095-004-9003-5>
2a. Harris J. M. in: Poly(ethylene glycol) Chemistry: Biotechnical and Biomedical Application (J. M. Harris, Ed.). Plenum Press, New York 1992.
2b. ACS Symp. Ser. 1997, 680, 458.
< X., Harris J. M.: https://doi.org/10.1021/bk-1997-0680.ch028>
3a. J. Macromol. Sci., Rev. Macromol. Chem. Phys. 1985, C25, 325.
< J. M.: https://doi.org/10.1080/07366578508081960>
3b. Bioconjugate Chem. 1995, 150.
< S.: https://doi.org/10.1021/bc00032a002>
4a. J. Bioactiv. Compat. Polym. 2001, 16, 206.
< G., Penczek S.: https://doi.org/10.1106/V7G8-R36H-BX1R-647G>
4b. J. Org. Chem. 2002, 67, 3096.
< Z., Ye S., Xia W.: https://doi.org/10.1021/jo025586h>
4c. Biomacromolecules 2003, 4, 1055.
< J., Kao W. J.: https://doi.org/10.1021/bm034069l>
4d. Bioactiv. Compat. Polym. 1989, 4, 17.
< K., Harris J. M.: https://doi.org/10.1177/088391158900400103>
4e. Tumor Target. Cancer Ther. 2002, 165.
< J. J., Page M.: https://doi.org/10.1385/1-59259-167-1:165>
5a. Makromol. Chem. 1981, 182, 1379.
< A. F., Morr M.: https://doi.org/10.1002/macp.1981.021820509>
5b. Tetrahedron 1987, 43, 4579.
< J.: https://doi.org/10.1016/S0040-4020(01)86900-3>
6. Macromol. Rapid Commun. 2003, 24, 681.
< P., Bonnans-Plaisance C., Jean M., Tassin J. F.: https://doi.org/10.1002/marc.200350012>
7a. Macromol. Chem. Phys. 1997, 198, 1009.
< M., Strohalm J., Ulbrich K., Schacht E.: https://doi.org/10.1002/macp.1997.021980408>
7b. Martinez A. J., Greenwald R. B.: U.S. 5605976; Chem. Abstr. 1997, 126, 225710.
7c. Macromol. Chem. Phys. 1998, 199, 247.
< M., Antonietti M., Cölfen H.: https://doi.org/10.1002/(SICI)1521-3935(19980201)199:2<247::AID-MACP247>3.0.CO;2-9>
7d. Synth. Commun. 2004, 34, 2309.
< A., Acton A., Lee-Ruff E.: https://doi.org/10.1081/SCC-120038518>
8a. Collect. Czech. Chem. Commun. 2004, 69, 1643.
< A., Pechar M., Ulbrich K.: https://doi.org/10.1135/cccc20041643>
8b. Tetrahedron Lett. 1977, 18, 1599.
< B., Bayer E.: https://doi.org/10.1016/S0040-4039(01)93225-3>
8c. Collect. Czech. Chem. Commun. 1995, 60, 1765.
< M., Strohalm J., Ulbrich K.: https://doi.org/10.1135/cccc19951765>
8d. Rosen P., Nho K.: U.S. 661,268; Chem. Abstr. 2004, 141, 157893.
9a. Finn R., Liao W., Siegel N.: U.S. 300,822; Chem. Abstr. 2004, 140, 241006.
9b. Macromol. Biosci. 2003, 3, 364.
< M., Ulbrich K., Jelínková M., Říhová B.: https://doi.org/10.1002/mabi.200350004>
9c. Bioorg. Med. Chem. Lett. 2001, 11, 2833.
< M., Buchta V., Kubicová L., Šimůnek P., Holčapek M., Kašparová P.: https://doi.org/10.1016/S0960-894X(01)00532-7>
10a. J. Polym. Sci., Part A: Polym. Chem. 1986, 24, 375.
< S., Harris J. M.: https://doi.org/10.1002/pola.1986.080240214>
10b. Org. Lett. 2000, 2, 3429.
< A., Taddel M.: https://doi.org/10.1021/ol0002222>
11a. J. Biomed. Mater. Res. 1992, 26, 779.
< K., Holmberg K.: https://doi.org/10.1002/jbm.820260607>
11b. Macromol. Chem. Phys. 2001, 202, 587.
< M., Cölfen H.: https://doi.org/10.1002/1521-3935(20010201)202:4<587::AID-MACP587>3.0.CO;2-F>
12a. React. Funct. Polym. 1997, 35, 135.
< G. R., Sharma S. D., Porath J., Guzman R. Z.: https://doi.org/10.1016/S1381-5148(97)00078-3>
12b. React. Funct. Polym. 2001, 48, 119.
< S., Benedetti F., Bonora G. M.: https://doi.org/10.1016/S1381-5148(01)00044-X>
13a. Org. Lett. 2002, 25, 4399.
< S., Narsihmulu C., Sultana S. S., Reddy N. R.: https://doi.org/10.1021/ol0266976>
13b. Tetrahedron Lett. 2004, 45, 5865.
< S., Narsihmulu C., Saritha B., Sultana S. S.: https://doi.org/10.1016/j.tetlet.2004.05.153>
13c. Curr. Org. Chem. 2005, 9, 195.
< C. K. Z., Alves L. M.: https://doi.org/10.2174/1385272053369178>
14a. J. Phys. Org. Chem. 2001, 14, 618.
< T., Palokangas J., Talvensaari M.: https://doi.org/10.1002/poc.411>
14b. J. Chem. Soc., Perkin Trans. 2 2001, 2314.
< D., Maia A., Pinna C.: https://doi.org/10.1039/b105877k>
15a. Chem. Rev. 1997, 97, 489.
< D. J., Janda K. D.: https://doi.org/10.1021/cr960064l>
15b. Haag R., Hebel A., Stumbè J. F. in: Handbook of Combinatorial Chemisty, Drugs, Catalysis, Materials (K. C. Nicolaou, R. Hanko and W. Hartwig, Eds), Vol. 1, p. 24. Wiley-VCH, Weinheim 2002.
16. Molecules 2000, 5, 1018.
< F., Wentworth P., Janda K. D.: https://doi.org/10.3390/50801018>
17a. Adv. Synth. Catal. 2001, 343, 171.
< M., Celentano G., Cozzi F.: https://doi.org/10.1002/1615-4169(20010226)343:2<171::AID-ADSC171>3.0.CO;2-3>
17b. Adv. Synth. Catal. 2002, 344, 533.
< M., Cinquini M., Cozzi F., Puglisi A., Celentano G.: https://doi.org/10.1002/1615-4169(200207)344:5<533::AID-ADSC533>3.0.CO;2-Y>
17c. J. Am. Chem. Soc. 1996, 118, 7632.
< H. S., Janda K. D.: https://doi.org/10.1021/ja9608095>
18a. J. Am. Chem. Soc. 1963, 85, 2149.
< R. B.: https://doi.org/10.1021/ja00897a025>
18b. Dörwald F. Z.: Organic Synthesis on Solid Phase, p. 25. Wiley-VCH, Weinheim 2002.
19a. Tetrahedron Lett. 2001, 42, 2257.
< O., Clapham B., Janda K. D.: https://doi.org/10.1016/S0040-4039(01)00172-1>
19b. Tetrahedron 2005, 61, 709.
< C. W. Y., Toy P. H.: https://doi.org/10.1016/j.tet.2004.10.108>
20. Tetrahedron Lett. 2002, 43, 9023.
< V. A., Siu M., Belanger J. M. R., Paré J. R. J.: https://doi.org/10.1016/S0040-4039(02)02306-7>
21a. Proc. Natl. Acad. Sci. USA 1995, 92, 6419.
< H., Wolfe M. M., Brenner S., Janda K. D.: https://doi.org/10.1073/pnas.92.14.6419>
21b. J. Am. Chem. Soc. 1996, 118, 2540.
H. S., Janda K. D.:
21c. J. Combinatorial Chem. 2002, 4, 359.
< P. M., Sun C. M.: https://doi.org/10.1021/cc0200080>
21d. Tetrahedron Lett. 2002, 43, 1725.
< J. Y., Sun C. M.: https://doi.org/10.1016/S0040-4039(02)00061-8>
21e. Tetrahedron Lett. 2003, 44, 4113.
< X. F., Zhang J., Wang Y. G.: https://doi.org/10.1016/S0040-4039(03)00852-9>
21f. Tetrahedron Lett. 2003, 44, 8939.
M. J., Sun C. M.:
21g. J. Combinatorial Chem. 2004, 6, 99.
< M., Fang J.: https://doi.org/10.1021/cc030034d>
21h. Synthesis 2005, 530.
W. G., Yang Y. Y., Wang Y. G.:
21i. J. Combinatorial Chem. 2004, 6, 279.
< W. B., Sun C. M.: https://doi.org/10.1021/cc034070o>
22a. Tauer K.: Reactive Surfactants, NATO ASI Ser., Ser. E, p. 463. Kluwer 1997.
22b. Macromol. Rapid Commun. 2001, 22, 219.
< H.: https://doi.org/10.1002/1521-3927(20010201)22:4<219::AID-MARC219>3.0.CO;2-G>
22c. Prog. Polym. Sci. 2003, 28, 1107.
< G.: https://doi.org/10.1016/S0079-6700(03)00015-7>
22d. Macromol. Rapid Commun. 2004, 25, 1478.
< J., Schlaad H.: https://doi.org/10.1002/marc.200400228>
22e. Adv. Polym. Sci. 2004, 165, 1.
< J., Eisenbach C. D., Jaeger W., Mori H., Müller A. H. E., Rehahn M., Schaller C., Traser S., Wittmeyer P.: https://doi.org/10.1007/b11266>
22f. Polymer 2005, 46, 1003.
< K., Imroz Ali A. M., Yildiz U., Sedlák M.: https://doi.org/10.1016/j.polymer.2004.11.036>
23. Chem. Eur. J. 1998, 4, 2493.
< M., Breulmann M., Göltner C. G., Cölfen H., Wong K. W., Walsh D., Mann S.: https://doi.org/10.1002/(SICI)1521-3765(19981204)4:12<2493::AID-CHEM2493>3.0.CO;2-V>
24. Bioconjugate Chem. 1995, 6, 639.
< A. V., Vinogradov S. V., Suzdaltseva Y. G., Alakhov V. Y.: https://doi.org/10.1021/bc00036a001>
25. Makromol. Chem. 1990, 191, 301.
< M., Anazawa H., Takahashi A., Inoue S.: https://doi.org/10.1002/macp.1990.021910204>
26a. Bioconjugate Chem. 1998, 9, 805.
< S. V., Bronich T. K., Kabanov A. V.: https://doi.org/10.1021/bc980048q>
26b. J. Controlled Release 2002, 81, 379.
< A., Chillon M., Leorgne C., Danos O., Frisch B.: https://doi.org/10.1016/S0168-3659(02)00080-9>
27a. Polym. Mater. Sci. Eng. 1997, 76, 54.
L., Sedlák M., Hartmann J., Cölfen H., Antonietti M.:
27b. Polym. Mater. Sci. Eng. 1999, 80, 124.
L., Sidorov S., Berton B., Sedlák M., Cölfen H., Antonietti M.:
28a. Mann S.: Biomimetic Material Chemistry. Wiley-VCH, Cambridge 1996.
28b. Angew. Chem., Int. Ed. 2003, 42, 2350.
< H., Mann S.: https://doi.org/10.1002/anie.200200562>
29. Chem. Eur. J. 2002, 8, 2429.
< Y., Sedlák M., Cölfen H., Antonietti M.: https://doi.org/10.1002/1521-3765(20020603)8:11<2429::AID-CHEM2429>3.0.CO;2-6>
30a. Biomaterials 2001, 22, 405.
< F. M.: https://doi.org/10.1016/S0142-9612(00)00193-9>
30b. Pharmazie 2002, 57, 5.
D., Bhadra S., Jain P., Jain N. K.:
30c. Cancer Treatment Rev. 2002, 28, 7.
< J.: https://doi.org/10.1016/S0305-7372(02)80003-2>
30d. Nat. Rev. Drug Discovery 2003, 2, 214.
< J. M., Chess R. B.: https://doi.org/10.1038/nrd1033>
30e. Adv. Drug Delivery Rev. 2004, 10, 91.
< N. V.: https://doi.org/10.1016/0169-409X(93)90005-O>
31a. Adv. Drug Deliv. Rev. 2002, 54, 571.
< K. R., Modi M. W., Pedder S.: https://doi.org/10.1016/S0169-409X(02)00028-5>
31b. Bioconjugate Chem. 2005, 16, 200.
< M. S., Doherty D. H., Smith D. J., Carlson S. J.: https://doi.org/10.1021/bc049713n>
31c. Tischer W.: WO 2003029291; Chem. Abstr. 2003, 138, 298131.
31d. Bioconjugate Chem. 2005, 16, 147.
< L. C., Lee H. F., Chung M. J., Yang V. C.: https://doi.org/10.1021/bc0499735>
32a. Crit. Rev. Ther. Drug Carrier Syst. 2000, 17, 101.
< R. B., Conover C. D., Choe Y. H.: https://doi.org/10.1615/CritRevTherDrugCarrierSyst.v17.i2.20>
32b. J. Controlled Release 2001, 74, 159.
< R. B.: https://doi.org/10.1016/S0168-3659(01)00331-5>
32c. Adv. Drug Delivery Rev. 2003, 55, 217.
< R. B., Choe Y. H., McGuire J., Conover C. D.: https://doi.org/10.1016/S0169-409X(02)00180-1>
33a. Biochim. Biophys. Acta 1992, 1113, 171.
< M. C., Lasie D. D.: https://doi.org/10.1016/0304-4157(92)90038-C>
33b. Curr. Pharm. Design 2004, 10, 2981.
< O. P., Zhu Y., Kairemo K.: https://doi.org/10.2174/1381612043383467>
34a. J. Controlled Release 1995, 34, 223.
< F. P., Montenegro L., Decapraiis P., Palagiano F., Trapani G., Liso G.: https://doi.org/10.1016/0168-3659(95)00003-Q>
34b. J. Biomater. Sci., Polym. Ed. 1997, 8, 741.
< L., Peroni P., Ferruti P., Latini R., Bernasconi R.: https://doi.org/10.1163/156856297X00281>
34c. Telyatnikov V. V., Guo Z., Schafer J.: WO 2004082620; Chem. Abstr. 2004, 141, 201467.
34d. Farmaco 2002, 57, 207.
< M., Luca G. D., Maurich V., Boccù E.: https://doi.org/10.1016/S0014-827X(01)01193-4>
34e. Pasut G., Veronese F.: WO 2004089420; Chem. Abstr. 2004, 141, 37851.
35a. Bioorg. Med. Chem. 1998, 6, 551.
< R. B., Pendri A., Conover C. D., Lee C., Choe Y. H., Gilbert C., Martinez A., Xia J., Wu D., Hsue M.: https://doi.org/10.1016/S0968-0896(98)00005-4>
35b. Bioorg. Med. Chem. Lett. 2003, 13, 577.
< R. B., Choe Y. H., Wu D.: https://doi.org/10.1016/S0960-894X(02)00926-5>
35c. Bioorg. Med. Chem. 2003, 13, 2635.
< R. B., Zhao H., Xia J.: https://doi.org/10.1016/S0968-0896(03)00152-4>
36a. J. Pharm. Sci. 1997, 86, 765.
< D., Nicholaou M. G., Borchardt R. T., Wang B.: https://doi.org/10.1021/js970069d>
36b. Bioorg. Med. Chem. 2003, 13, 2531.
< Z., Zhang H., Huang J.: https://doi.org/10.1016/S0960-894X(03)00470-0>
37a. Bioconjugate Chem. 2003, 14, 563.
< O., Horowitz A. T., Gabizon A., Gibson D.: https://doi.org/10.1021/bc025642l>
37b. Adv. Drug Delivery Rev. 2004, 56, 1023.
< K., Šubr V.: https://doi.org/10.1016/j.addr.2003.10.040>
37c. J. Med. Chem. 1999, 42, 3657.
< R. B., Pendri A., Conover C. D., Zhao H., Choe Y. H., Martinez A., Shum K., Guan S.: https://doi.org/10.1021/jm990166e>
37d. J. Med. Chem. 2004, 47, 726.
< R. B., Zhao H., Yang K., Reddy P., Martinez A.: https://doi.org/10.1021/jm030369+>
37e. Mol. Pharmacol. 2004, 1, 375.
< A. V., Hiller A., Syed S., Yin M., Lu X. M., Fischman A. J., Papisov M. I.: https://doi.org/10.1021/mp0499306>
38a. Org. Biomol. Chem. 2003, 1, 1204.
< M., Hanusek J., Hejtmánková L., Kašparová P.: https://doi.org/10.1039/b209107k>
38b. Org. Biomol. Chem. 2004, 2, 562.
< P., Mindl J., Štěrba V., Hanusek J.: https://doi.org/10.1039/b310454k>
38c. Org. Biomol. Chem. 2004, 2, 1756.
< J., Hejtmánková L., Štěrba V., Sedlák M.: https://doi.org/10.1039/b401866d>
39a. Macromol. Chem. 1989, 190, 2041.
< M., Inoue S., Kataoka K., Yui N., Okano T., Sakurai Y.: https://doi.org/10.1002/macp.1989.021900904>
39b. Adv. Drug Delivery Rev. 1997, 26, 151.
< I., Springer C. J.: https://doi.org/10.1016/S0169-409X(97)00032-X>
39c. Curr. Opin. Mol. Ther. 1999, 1, 480.
I., Cooper R. G., Stribbling S. M., Heyes J. A., Metacalfe J. A., Springer C. J.:
40a. New Engl. J. Med. 1992, 82, 662.
M. S., Powderly W. G., Cloud G. A., Brune H. K., Sabra R.:
40b. Holz R. W. in: Antibiotics (F. E. Hahn, Ed.), Vol. 5, p. 313. Springer, Berlin 1979.
40c. Int. J. Pharm. 2000, 201, 37.
< K., Mararuyama K., Iwatsuru M.: https://doi.org/10.1016/S0378-5173(00)00391-4>
40d. Kubicová L., Pravda M., Buchta V., Vopršálová M., Sedlák M.: Centr. Eur. J. Publ. Health 2004, Suppl. 53.
40e. Bioconjugate Chem. 2003, 14, 661.
< C. D., Zhao H., Longley C. B., Shun K. L., Greenwald R. B.: https://doi.org/10.1021/bc0256594>
41a. Drug Future 2003, 28, 1198.
< B.: https://doi.org/10.1358/dof.2003.028.12.857390>
41b. Chem. Listy 2004, 98, 1073.
S.:
41c. Chem. Listy 2004, 98, 1087.
L., Fusek M.: