A facile, viable, "green" two-step, inexpensive technique was developed for the preparation of (32)P patch for the treatment of skin cancer. This technique consists of impregnation of H(3)(32)PO(4) solution into an inert solid carrier followed by immobilization into a nonleachable matrix by lamination. The morphology of the impregnated paper was evaluated by scanning electron microscope and energy-dispersive spectral analyses. Radioactive patches containing up to ∼37 MBq/cm(2) of (32)P could be prepared. Distribution of (32)P on sources was uniform and release of (32)P from the sealed source in water and saline was found to be well within the permissible levels of 185 Bq. Custom-shaped (32)P-patches after quality assurance were supplied to AIIMS, New Delhi, for clinical evaluation. (32)P-impregnated paper protected by a laminated film holds promise for treatment of superficial cancers.

Download full-text PDF

Source
http://dx.doi.org/10.1089/cbr.2011.0979DOI Listing

Publication Analysis

Top Keywords

facile viable
8
preparation 32p
8
treatment skin
8
skin cancer
8
32p
5
viable approach
4
approach preparation
4
32p patches
4
patches treatment
4
cancer facile
4

Similar Publications

Controlling Microparticle Aspect Ratio via Photolithography for Injectable Granular Hydrogel Formation and Cell Delivery.

ACS Biomater Sci Eng

January 2025

Weldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.

Granular hydrogels are injectable and inherently porous biomaterials assembled through the packing of microparticles. These particles typically have a symmetric and spherical shape. However, recent studies have shown that asymmetric particles with high aspect ratios, such as fibers and rods, can significantly improve the mechanics, structure, and cell-guidance ability of granular hydrogels.

View Article and Find Full Text PDF

In this paper, we present a facile yet effective method for the fabrication of core-shell nanoparticles (NPs) of magnetite (FeO) and polydopamine (FeO@PDA) and their decoration with a tunable amount of gold NPs (AuNPs). For this, FeO NPs were fabricated through the polyol method and AuNPs were deposited onto FeO@PDA via anchoring of as-prepared citrate-stabilized AuNPs or reduction of Au ions. PDA with its numerous catechol groups enabled the decoration of AuNPs in a well-controlled manner.

View Article and Find Full Text PDF

Electrochemical Dicarboxylation of Vinyl Epoxide with CO for the Facile and Selective Synthesis of Diacids.

Angew Chem Int Ed Engl

December 2024

State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, China.

We present a novel electrochemical dicarboxylation of epoxides with CO, characterized by the cleavage of two C-O single bonds. Not only are vinyl epoxides viable, but cyclic carbonates also serve as effective substrates, facilitating the synthesis of E-configured adipic and octanedioic acids with high chemo-, regio-, and stereoselectivity. The synthetic practicality is further highlighted by the diverse functionalizations of the resulting multifunctional diacids.

View Article and Find Full Text PDF

The realization of higher coupling strengths between coupled resonant modes enables exploration of compelling phenomena in diverse fields of physics and chemistry. In this study, we focus on the modal coupling between localized surface plasmon resonance (LSPR) of Au nanoparticles (Au-NPs) and Fabry-Pérot mode (p-NiO/Au film). The effects of nanoparticle size, projected surface coverage (PSC), interparticle distance (IPD), and arrangement to the coupling strength between the two modes are theoretically investigated using finite-difference time-domain (FDTD) method.

View Article and Find Full Text PDF
Article Synopsis
  • Crystalline-amorphous hybrid materials, specifically CoNi-layered double hydroxides (CA-CoNi-LDHs), have been developed for improved energy storage, overcoming challenges in regulating their structure.
  • The experimental approach involves a simple electrochemical activation method that enhances both the morphology and electronic properties of these materials, leading to more active sites for energy storage due to increased defect density and active species concentration.
  • The resulting CA-CoNi-LDHs@CC electrode demonstrates impressive performance metrics, such as an areal capacitance of 13,070 mF/cm² and high energy density of 0.71 mWh/cm², showcasing the effectiveness of these hybrid materials for energy applications.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!