Keyword search (4,163 papers available)

"Pawelek PD" Authored Publications:

Title Authors PubMed ID
1 The enterobactin biosynthetic intermediate 2,3-dihydroxybenzoic acid is a competitive inhibitor of the Escherichia coli isochorismatase EntB Bin X; Pawelek PD; 40400396
CHEMBIOCHEM
2 Evidence of isochorismate channeling between the Escherichia coli enterobactin biosynthetic enzymes EntC and EntB Bin X; Pawelek PD; 39031458
CHEMBIOCHEM
3 Evidence of an intracellular interaction between the Escherichia coli enzymes EntC and EntB and identification of a potential electrostatic channeling surface Ouellette S; Pakarian P; Bin X; Pawelek PD; 35952947
CHEMBIOCHEM
4 A shared binding site for NAD+ and coenzyme A in an acetaldehyde dehydrogenase involved in bacterial degradation of aromatic compounds. Lei Y, Pawelek PD, Powlowski J 18537268
CHEMBIOCHEM
5 Subunit orientation in the Escherichia coli enterobactin biosynthetic EntA-EntE complex revealed by a two-hybrid approach. Pakarian P, Pawelek PD 27086082
CHEMBIOCHEM
6 Intracellular co-localization of the Escherichia coli enterobactin biosynthetic enzymes EntA, EntB, and EntE. Pakarian P, Pawelek PD 27470582
CHEMBIOCHEM
7 A novel set of vectors for Fur-controlled protein expression under iron deprivation in Escherichia coli. Pakarian P, Pawelek PD 27619907
CHEMBIOCHEM
8 Dual Activity of Rose Bengal Functionalized to Albumin-Coated Lanthanide-Doped Upconverting Nanoparticles: Targeting and Photodynamic Therapy. Sabri T, Pawelek PD, Capobianco JA 30028124
CNSR

 

Title:Dual Activity of Rose Bengal Functionalized to Albumin-Coated Lanthanide-Doped Upconverting Nanoparticles: Targeting and Photodynamic Therapy.
Authors:Sabri TPawelek PDCapobianco JA
Link:https://www.ncbi.nlm.nih.gov/pubmed/30028124?dopt=Abstract
Publication:
Keywords:
PMID:30028124 Category:ACS Appl Mater Interfaces Date Added:2019-05-31
Dept Affiliation: CNSR
1 Department of Chemistry and Biochemistry and Centre for NanoScience Research , Concordia University , 7141 Sherbrooke Street West , Montreal , Quebec H4B 1R6 , Canada.

Description:

Dual Activity of Rose Bengal Functionalized to Albumin-Coated Lanthanide-Doped Upconverting Nanoparticles: Targeting and Photodynamic Therapy.

ACS Appl Mater Interfaces. 2018 Aug 15;10(32):26947-26953

Authors: Sabri T, Pawelek PD, Capobianco JA

Abstract

A modified version of a desolvation method was used to render lanthanide-doped upconverting nanoparticles NaGdF4:Yb3+/Er3+ (Ln-UCNPs) water-dispersible and biocompatible for photodynamic therapy. Bovine serum albumin (BSA) was used as surface coating with a direct conjugation to NaGdF4:Yb3+/Er3+ nanoparticles forming a ~2 nm thick shell. It was estimated that approximately 112 molecules of BSA were present and cross-linked per NaGdF4:Yb3+/Er3+ nanoparticle. Analysis of the BSA structural behavior on the Ln-UCNP surfaces displayed up to 80% loss of a-helical content. Modification of the Ln-UCNPs with a BSA shell prevents luminescence quenching from solvent molecules (H2O) with high energy vibrations that can interact with the excited states of the optically active ions Er3+ and Yb3+ via dipole-dipole interactions. Additionally, the photosensitizer rose bengal (RB) was conjugated to albumin on the surface of the Ln-UCNPs. Emission spectroscopy under 980 nm excitation was carried out, and an energy transfer efficiency of 63% was obtained. In vitro cell studies performed using human lung cancer cells (A549 cell line) showed that Ln-UCNPs coated with BSA were not taken by the cells. However, when RB was conjugated to BSA on the surface of the nanoparticles, cellular uptake was observed, and cytotoxicity was induced by the production of singlet oxygen under 980 nm irradiation.

PMID: 30028124 [PubMed - indexed for MEDLINE]





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