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தொகுதி 13, பிரச்சினை 7 (2022)

மினி விமர்சனம்

Developments in the Analysis for Borderline Resectable and Sectionally Advanced Exocrine Gland Adenocarcinoma

Taylor Lee

Pancreatic ductal adenocarcinoma (PDAC) stays quite possibly of the deadliest threat in the United States. Enhancements in imaging have allowed the classification of patients as per radiologic contribution of encompassing vasculature, i.e., forthright resectable, fringe resectable, and privately progressed sickness, and this, thus, has affected the arrangement of chemotherapy, medical procedure, and radiation treatment. However careful resection stays the main healing treatment choice, late investigations have shown better by and large endurance with neoadjuvant chemotherapy, particularly among patients with fringe resectable/privately progressed sickness. The job of radiologic imaging after neoadjuvant treatment and the likely advantage of adjuvant treatment for fringe resectable and privately progressed sickness remain areas of continuous examination. The advances made in the therapy of patients with fringe resectable/privately progressed sickness are promising, yet differences in admittance to malignant growth care continue. This audit features the critical advances that have been made in the treatment of fringe resectable and privately progressed PDAC, while additionally pointing out the excess difficulties. View Full-Text

மினி விமர்சனம்

Effective Analytical Target Capacity of Radiotherapy Based on Minute Protract in Non-tiny-cell Pulmonary Cancer

Huang Zhao

A pivotal issue in revolutionary radiation treatment for non-little cell cellular breakdown in the lungs is the manner by which to characterize the clinical objective volume (CTV). Albeit the extent of infinitesimal expansion (ME) and minuscule proximal bronchial augmentation (PBE) from an essential growth ought to be thought about while characterizing the CTV, there has been restricted examination on ME and PBE. Hence, we directed this orderly audit. The PubMed, ICHUSHI (Japanese information base), and Cochrane Library data sets were looked, and 816 articles were at first recovered. After essential and auxiliary screenings, eight articles were eventually chosen. The consequences of this orderly survey propose the significance of a 0 mm edge in stereotactic radiotherapy for beginning phase malignant growth and a 5-8 mm edge in healing illumination for privately progressed disease. Concerning, this audit yielded the end that it is suitable to consider the expansion of an around 15 mm edge from the bronchial vasculature. In spite of the fact that there were not many articles with an elevated degree of proof, this deliberate survey empowered us to examine results from past examinations and to give suggestions, somewhat, in regards to the CTV edge in the ongoing clinical climate, where high-accuracy radiation treatment, for example, picture directed radiotherapy and power tweaked radiotherapy, is overwhelming.

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Boron Neutron Capture Therapy of Mcf-7 Breast Cancer Cells by Using Calcium Fructoborate@Au Nanoparticles Drug Encapsulated in Liposomal Nanocarriers: In-vitro Experimental Investigation

Meisam Sadeghi Zahra Moghimifar and Hamedreza Javadian2

In this research, calcium fructoborate (CFB) complex containing enriched 10B was used as a drug. The liposome prepared from phosphatidylcholine was applied as a biological macromolecule carrier of the drug. The liposome-encapsulated CFB (LECFB) was applied to treat MCF-7 breast cancer cells. The study demonstrated that AuNPs added to LECFB in the core-shell structure of LECFB with AuNPs (LECFB@AuNPs) can be considered selectively for the specific biological labeling and delivery of large quantities of boron to the cancer cells, respectively. Polyethylene glycol (PEG) and folic acid (FA) were chosen as appropriate substrates to potentially attach to folate receptors (FR) on the surface of cancer cells before liposomal formulation. The size of folate-conjugated LECFB@AuNPs was around 240.9 nm, while the size of synthesized LECFB was 142.3 nm. The optimum encapsulation efficiency was 72.38 ± 1.68% under the conditions of T=60°C, drug:lipid ratio=1:5, and incubation time=60 min. PEGylated liposome improved 0.07 mg of the drug loading content, and the amounts of the drug release from PEGylated formulation at 37 and 42 °C were respectively 8.89 and 5.78% more than those obtained by the optimum formula of the drug encapsulation.

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