ANTI-PROLIFERATIVE POTENTIAL OF Carica papaya LEAVES ON BREAST CANCER CELLS – MCF-7

The study's objective is to identify the phytoconstituents and determine the anti-cancer potential of Carica papaya leaves against the MCF 7 cell line. Chloroform, ethyl acetate, and methanol extracts of C. papaya leaves were prepared by cold maceration method and qualitative phytochemical analysis was performed. The anti-proliferative effect of these extracts was determined by 3-(4,5- dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay and apoptotic assay by acridine orange/ethidium bromide staining method on MCF 7 cells.  The effect of the extracts, with different concentrations, on DNA fragmentation, was also performed on MCF 7 cells. Qualitative analysis revealed the presence of alkaloids, flavonoids, terpenoids, steroids, saponins, tannins, glycosides, phenols, anthraquinones, proteins, and carbohydrates. Chloroform, methanol, and ethyl acetate extracts of C. papaya leaves were observed with potential DPPH free radical scavenging activity with 72%, 75%, and 78% respectively. Of these extracts, the chloroform extract (72%) was found to possess a more free radical scavenging effect against DPPH and also showed a dose-dependent effect, the maximum at 100µg/ml, on DNA fragmentation in MCF 7 cells. Further, chloroform extract showed a maximum anti-proliferative effect on MCF-7 cells with IC50 at 22±1.5µg/ml, whereas methanol and ethyl acetate extract at 30±0.5 µg/ml and 28±0.5 µg/ml respectively.  Increased apoptosis in MCF 7 cells was observed with an increased concentration of chloroform extract of C. papaya. From the results of this study, it can be concluded that leaf extract of C. papaya found to possess an anti-proliferative effect and antioxidant potential and it could be due to the presence of rich secondary metabolites of the plant

Characterization of WO3 thin films deposited by spray pyrolysis technique and its role in gas sensing

The work investigated in this paper focused on the fabrication of WO3 films by the spray pyrolysis technique, and different analyses were made to find optimized samples for studying properties suitable for the application of gas sensing. The substrate temperature is the most important parameter among other spray parameters for the synthesis of thin films hence WO3 thin films were deposited on glass substrates by maintaining the substrate temperature at 350 ºC, 450 ºC, 550 ºC, and 650 °C using compressed air as a carrier gas. The influence of the substrate temperature on the structural, morphological, compositional, and optical properties of the WO3 thin films has been justified using XRD data. Good and enhanced crystallinity is observed for the film deposited at a substrate temperature of 550 ºC. The nonconventional properties were studied by different investigations and confirmed by past research work. The manipulation of surface morphology with the different deposition temperatures is monitored. Only the characteristic peaks of W and O are present in the fabricated WO3 thin films. The optical activity of about 70 to 80 % of the selected sample in the visible region (300 to 1200 nm) is found. The selective absorption activity of light in the ultraviolet region and visible region is checked. The obtained IR bands confirmed the inter bridge stretching and bending modes of W-O and O-W-O. A high response towards ammonia compared to other test gases is exhibited. The repeatability of WO3 towards NH3 over three periodic sensing cycles, response, and recovery time has also been discussed. From all the characteristic studies, it has been suggested that the fabricated WO3 thin films have been used in the health care field to detect the toxic NH3 ga

Ethyl 4′-ethenyl-2′-oxo-4-phenyl-2-(3,4,5-trimethoxy­phen­yl)spiro­[pyrrolidine-3,3′-indoline]-5-carboxyl­ate monohydrate

In the title compound, C31H32N2O6·H2O, the pyrrolidine ring adopts an envelope conformation. The ethyl C atoms of the ethoxy­cabonyl group are disordered over two positions with occupancies of ca 0.80 and 0.20. Intra­molecular N—H⋯O hydrogen bonds form S(5) and S(6) ring motifs. Mol­ecules are linked into a three-dimensional framework by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds, and by C—H⋯π inter­actions

Effect of okra plant resistance on transmission rate of okra enation leaf curl virus by its vector whitefly, Bemisia tabaci

The present study aimed to investigate the effect of age of the okra plants that showed varying whitefly resistance responses on the transmission rate of okra enation leaf curl virus (OELCV) by its vector whitefly Bemisia tabaci. The OELCV infected whitefly adults were collected from whitefly colonies and were challenged on the test okra accessions (Upl mona 2, Co 1, Arka anamika and AE 64) of differential ages which were individually caged (7, 10 and 15 d after germination) with glass chimney and the number of such whiteflies used were at the rate of 2, 4, 6, 8, 10, 12, 14 and 20 adults per plant. Observations were made on the virus symptom expression 30 d after challenge. The efficiency of transmission was determined. The efficiency of transmission of OELCV was the highest (maximum T and P*, 0.80, 1.00 and 0.08, 0.10) when 7 d old seedlings were inoculated (Arka anamika and AE 64 respectively) and transmission had decreased as the age of seedlings increased. The estimated transmission rate for single whitefly (P*) increased with an increase in the number of whiteflies used per plant. Okra plant resistance to B. tabaci significantly changed the transmission rates of OELCV on okra. Understanding the resistance mechanisms of the okra accessions and interactions between plant viruses and their insect host can pave the way for novel approaches to protect plants from virus infection

Prevalence of copepod parasite (Lernaeenicus polynemi) infestation on Eleutheronema tetradactylum from Pazhayar coastal waters, southeast coast of India

Objective: To study the prevalence and mean intensity of copepod parasite Lernaeenicus polynemi infestation on Eleutheronema tetradactylum from Pazayar, Tamil Nadu, of India. southeast coast Methods: The fish was collected from Pazhayar landing centre from January to December 2012 aonf dp atrhaesiirt ebsi owmeeretr rice cmoredaesdu.rements were examined. Toal number of infected fish and total number. Results: Higher prevalence and mean intensity of infestation of 35.23% and 3.1 were respectively rbeopdoyr toefd t hdeu rhinosgt manodn stoaorgne steedas tohne odfi f2f0e1r2e.n Tt hinet epranraals iotircg ainnsfe ssutacthio anss lwiveerre asncda tttheree ddo orvsaelr athoret ae.n Ttihree highest intensity was reported to be 66 parasites in a single host. Conclusions: Due to the heavy parasitic attack the fish will suffer and its economical value or the marketability may reduce

Bioprinting and biomaterials for dental alveolar tissue regeneration

Three dimensional (3D) bioprinting is a powerful tool, that was recently applied to tissue engineering. This technique allows the precise deposition of cells encapsulated in supportive bioinks to fabricate complex scaffolds, which are used to repair targeted tissues. Here, we review the recent developments in the application of 3D bioprinting to dental tissue engineering. These tissues, including teeth, periodontal ligament, alveolar bones, and dental pulp, present cell types and mechanical properties with great heterogeneity, which is challenging to reproduce in vitro. After highlighting the different bioprinting methods used in regenerative dentistry, we reviewed the great variety of bioink formulations and their effects on cells, which have been established to support the development of these tissues. We discussed the different advances achieved in the fabrication of each dental tissue to provide an overview of the current state of the methods. We conclude with the remaining challenges and future needsThis work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI (Grant Numbers 22K18936 and 21K04852); AMED (Grant Number JP21gm1310001); The JST Adaptable and Seamless Technology Transfer Program through Target-driven R&D (Grant Number JPMJTM22BD), CASIO SCIENCE PROMOTION FOUNDATION, and by the Research Center for Biomedical Engineering at Tokyo Medical and Dental University, Japan

Hybrid hydrogels containing vertically aligned carbon nanotubes with anisotropic electrical conductivity for muscle myofiber fabrication

Biological scaffolds with tunable electrical and mechanical properties are of great interest in many different fields, such as regenerative medicine, biorobotics, and biosensing. In this study, dielectrophoresis (DEP) was used to vertically align carbon nanotubes (CNTs) within methacrylated gelatin (GelMA) hydrogels in a robust, simple, and rapid manner. GelMA-aligned CNT hydrogels showed anisotropic electrical conductivity and superior mechanical properties compared with pristine GelMA hydrogels and GelMA hydrogels containing randomly distributed CNTs. Skeletal muscle cells grown on vertically aligned CNTs in GelMA hydrogels yielded a higher number of functional myofibers than cells that were cultured on hydrogels with randomly distributed CNTs and horizontally aligned CNTs, as confirmed by the expression of myogenic genes and proteins. In addition, the myogenic gene and protein expression increased more profoundly after applying electrical stimulation along the direction of the aligned CNTs due to the anisotropic conductivity of the hybrid GelMA-vertically aligned CNT hydrogels. We believe that platform could attract great attention in other biomedical applications, such as biosensing, bioelectronics, and creating functional biomedical devices

(Z)-3-(4-Fluoro­phen­yl)-1-[4-(methyl­sulfon­yl)phen­yl]-2-tosyl­prop-2-en-1-one

In the title compound, C23H19FO5S2, two of the phenyl ring C atoms and a sulfonyl O atom of the phenyl(methylsulfonyl) group are disordered over two positions with occupancies 0.522 (17):0.478 (17). The methyl­phenyl and fluoro­phenyl rings are essentially planar, with maximum deviations of 0.0059 (8) and 0.0047 (9) Å, respectively. The crystal packing is stabilized by C—H⋯F inter­actions

3D Bioprinting tissue analogs: Current development and translational implications

Three-dimensional (3D) bioprinting is a promising and rapidly evolving technology in the field of additive manufacturing. It enables the fabrication of living cellular constructs with complex architectures that are suitable for various biomedical applications, such as tissue engineering, disease modeling, drug screening, and precision regenerative medicine. The ultimate goal of bioprinting is to produce stable, anatomically-shaped, human-scale functional organs or tissue substitutes that can be implanted. Although various bioprinting techniques have emerged to develop customized tissue-engineering substitutes over the past decade, several challenges remain in fabricating volumetric tissue constructs with complex shapes and sizes and translating the printed products into clinical practice. Thus, it is crucial to develop a successful strategy for translating research outputs into clinical practice to address the current organ and tissue crises and improve patients' quality of life. This review article discusses the challenges of the existing bioprinting processes in preparing clinically relevant tissue substitutes. It further reviews various strategies and technical feasibility to overcome the challenges that limit the fabrication of volumetric biological constructs and their translational implications. Additionally, the article highlights exciting technological advances in the 3D bioprinting of anatomically shaped tissue substitutes and suggests future research and development directions. This review aims to provide readers with insight into the state-of-the-art 3D bioprinting techniques as powerful tools in engineering functional tissues and organs