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. Author manuscript; available in PMC: 2018 Jul 15.
Published in final edited form as: Int J Pharm. 2017 May 22;527(1-2):79–91. doi: 10.1016/j.ijpharm.2017.05.045

Table 1.

Characterization of dendrimer-based compounds.

Compounds y M MW (Da) HD ± s.d. (nm) PDI ζ ± s.d. (mV)

1HNMR MALDI 1HNMR MALDI
G4OH - - - - 14374 4.5 ± 1.9 0.121 -0.1±0.4
G4OH-yNH2 5.8 6.3 - - 15091 4.1 ± 1.6 0.107 +13.2±4.9
Pep4 - - - 1363 9.6 ± 4.2 0.225 +17.4±9.0
G4OH-mPep4 2.7* 2.9** 3.1 3.4 19723 6.1 ± 2.5 0.163 +15.7±6.5
G4OH+Pep4 - - - - - 5.4 ± 1.9 0.159 +19.5±10.8

Note: Number of peripheral -NH2 groups of G4OH (y), number of Pep4 conjugated to G4OH (m), molecular weight (MW), hydrodynamic diameter (HD) and zeta potential of the dendrimers (G4OH and G4OH-yNH2), Pep4, G4OH-mPep4 conjugate and G4OH+Pep4 mixture as determined by 1HNMR, MALDI-TOF, and dynamic light scattering (DLS).

*

number of NH2 groups remaining after conjugation of Pep4 as determined by 1HNMR;

**

number of NH2 groups remaining after conjugation of Pep4 as determined by MALDI-TOF. PDI=polydispersity index.