Conjugation, macromolecular

Maeda H. SMANCS and polymer-conjugated macromolecular drugs advantages in cancer chemotherapy. Adv Drug Deliv Rev 1991 6 181-202. 

Maeda, H., 1994, Polymer conjugated macromolecular drugs for tumor-specific targeting. In Polymer Site Specific Pharmacotherapy (A. J. Domb, eds.) John Wiley Sons Ltd., New York, USA, pp. 95-116. 

Figure 2.2 Overview of ultrarapid and mild conjugation chemistries. (Reproduced with permission from A.J. Inglis and C. Earner-Kowollik, Ultra rapid approaches to mild macromolecular conjugation, Macromolecular Rapid Communications, 2010, 31,14,1247-1266. Wiley-VCH Verlag GmbH Co. KGaA.)...

Figure 8.12 The SEC analysis of the PiBA star-shaped polymer, P(EtOx)2o and the coupling product before (bottom) and after preparative SEC (top) (Lammens et al, 2009). (Reprinted from M. Lammens, D. Fournier, M.W.M. Fijten et aL, Star-shaped poly acrylates Highly functionalized architectures via CuAAC click conjugation, Macromolecular Rapid Communications, 30, 23, 2049-2055 (Table 2, Figure 3), 2009, with the permission of John Wiley Sons, Inc.)...

Lammens, M., Fournier, D., Fijten, M.W.M., Hoogenboom, R., and Du Prez, F. (2009) Star-shaped polyacrylates Highly functionalized architectures via CuAAC click conjugation. Macromolecular Rapid Communications, 30,2049. 

Stalmach, U., de Boer, B., Post, A.D. et al. (2001) Synthesis of a conjugated macromolecular initiator for nitroxide-mediated free radical polymerization. Angewandte Chemie International Edition, 40,428. 

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