Adah Almutairi

Synthesis and photochromic properties of molecules containing [e]-annelated dihydropyrenes. Two and three way pi-switches based on the dimethyldihydropyrene-metacyclophanediene valence isomerization.

Helical sexithiophenes: an experimental and theoretical study implicating the alternating 2,2':3,3' regioisomer as a reliable helical motif.

Biodegradable pH-sensing dendritic nanoprobes for near-infrared fluorescence lifetime and intensity imaging.

Enhanced cell penetration of acid-degradable particles functionalized with cell-penetrating peptides.

Biodegradable dendritic positron-emitting nanoprobes for the noninvasive imaging of angiogenesis.

Monitoring the biodegradation of dendritic near-infrared nanoprobes by in vivo fluorescence imaging.

Engineering NIR dyes for fluorescent lifetime contrast.

UV and near-IR triggered release from polymeric nanoparticles.

Multiresponse strategies to modulate burst degradation and release from nanoparticles.

NMR-derived models of amidopyrine and its metabolites in complexes with rabbit cytochrome P450 2B4 reveal a structural mechanism of sequential N-dealkylation.

Application of fiber-optic attenuated total reflection-FT-IR methods for in situ characterization of protein delivery systems in real time.

Inflammation responsive logic gate nanoparticles for the delivery of proteins.

Low power, biologically benign NIR light triggers polymer disassembly.

Density gradient multilayer polymerization for creating complex tissue.

Photochemical mechanisms of light-triggered release from nanocarriers.

Increasing materials' response to two-photon NIR light via self-immolative dendritic scaffolds.

Physical and chemical strategies for therapeutic delivery by using polymeric nanoparticles.

An Extracellular MRI Polymeric Contrast Agent That Degrades at Physiological pH.

Triggered rapid degradation of nanoparticles for gene delivery.

Iron oxide nanoparticle-based magnetic resonance method to monitor release kinetics from polymeric particles with high resolution.

Biocompatible polymeric nanoparticles degrade and release cargo in response to biologically relevant levels of hydrogen peroxide.

Antigen-loaded pH-sensitive hydrogel microparticles are taken up by dendritic cells with no requirement for targeting antibodies.

A Single UV or Near IR Triggering Event Leads to Polymer Degradation into Small Molecules.