Sentence examples for molecules and targeting from inspiring English sources

These dendrimers take advantage of a dendritic display to carry multiple drug molecules and targeting moieties simultaneously.

Moreover, by replacing the LoADing molecules and targeting strategies, this system can be applied for other specific genome engineering purposes, such as introducing longer deletions for gene disruption, independently introducing multiple mutations without chromosomal deletion, and efficiently incorporating a single-stranded oligodeoxynucleotide donor.

One of the most studied nanostructures in medicine are gold NPs (AuNPs), which can be constructed in different sizes and shapes, and have the ability to be decorated with drug molecules and targeting moieties.

An increase in size after subsequent surface modifications reflects the successful addition of NOTA, PEG molecules and targeting moieties on the surface of MSN at each step (Table 1).

By modifying these MCNPs with PEG molecules and targeting ligands such as iRGD, we were also able to overcome the critical obstacles impeding the clinical applications of ATAP as a cancer therapeutic, namely, poor aqueous solubility and lack of tumor-homing capacity.

Major challenges in designing chemistries to incorporate drug molecules and targeting moieties include compatibility of the carrier and the drug, carrier induced immunogenic responses, unbalanced increase in lipophilicity, stability and activity of the drug, and the number of available attachment sites for drug conjugation.

Much research in the program focuses on basic molecular interactions between drug molecules and target proteins in order to provide fundamental information that will lead to the discovery of more selective and effective therapeutic approaches to disease management.

The drug-target network was constructed according to the various binding data between molecules and target proteins.

CVDHD comprises six data entities covering medicinal herbs, natural products, target proteins, docking results between all molecules and target proteins, diseases and clinical biomarkers (Figure 1).

The proposed method can be used, as soon as drug molecules and target proteins can be represented by descriptors (chemical substructures and protein domains in this study).

FA-CHI-5-FAM is prepared by bonding the fluorescent molecule 5-FAM and targeting molecule FA to CHI through a reaction between the carboxyl groups of FA, 5-FAM and the amino groups of the CHI chain.