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Toward this objectives, we propose, synthesis of poly ethylene glycol) (PEG doxorubicin (DOX) prodrug conjugates consisting N-acetyl glucosamine (NAG) as a targeting moiety.
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Figure 1 shows the proposed synthesis diagram.
The proposed synthesis method is a simple and direct approach.
When successful, the simulations also provide a proposed synthesis pathway to the compound under study.
The same structure with just one different part was also implemented for the proposed synthesis system.
Finally, we present evaluation results that validate the potential benefits of our proposed synthesis method.
A simple schematic of the proposed synthesis has been illustrated in Fig. 1.
A numerical simulation is presented and shows the advantage of the proposed synthesis method.
A simple schematic of the proposed synthesis is illustrated in Fig. 1.
The objective of this analysis is to identify the hazards and risks of the proposed synthesis.
A numerical application corroborating the applicability of the proposed synthesis technique is also presented.
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