scholarly journals Effects of Different Irradiation Treatments on Total Saponins Content of Sapindus mukorossi

Dose-Response ◽  
2022 ◽  
Vol 20 (1) ◽  
pp. 155932582110627
Author(s):  
Yu-Min Shi ◽  
Heng Yan ◽  
Lin-Sen Wu ◽  
Jia-Jia Xie ◽  
Hong-Guo Chen
Keyword(s):  
Crude Extract ◽  
Low Dose ◽  
Reference Data ◽  
Biological Activities ◽  
Radical Scavenging ◽  
Ionic Surfactant ◽  
Γ Irradiation ◽  
Before And After ◽  
Γ Ray ◽  
Further Development

Sapindus mukorossi Gaertn is also known as Mu Huanzi, You Huanzi, soap tree, etc. The pericarp of  Sapindus mukorossi contains many saponins, which is a type of natural non-ionic surfactant. Its extract has vigorous surface activity and biological activities such as bacteriostasis, oxidation resistance, and free radical scavenging. The  Sapindus mukorossi extract is an environmentally friendly washing product that microorganisms can be rapidly decompose in nature without any environmental pollution.This study aims to investigate the effects of E-beam and Co60-γ irradiation on the total saponins content in the crude extract of the  S mukorossi. The  S mukorossi powder is irradiated with E-beam and Co60-γ ray at doses of 0, 4, 6, 8, 10, and 12 kGy for E-beam and 0, 50, 100, 150, and 200 Gy, respectively, for Co60-γ ray. The changes in the content of total saponins in the crude extract, total detergency, and the bacteriostatic abilities before and after the irradiation were analyzed. The results showed that the content of total saponins in samples irradiated by E-beam was significantly higher than that in non-irradiated samples. The saponins yield was the highest at a radiation dose of 6 kGy, and the detergency and bacteriostatic ability were also the strongest. After low-dose Co6-γ irradiation, the total saponins in the  S mukorossi crude extract, and detergency and bacteriostatic ability had no apparent change. Conclusion: E-beam irradiation at a dose of 6 kGy can effectively improve the content of total saponins in the crude extract of  S mukorossi powder. In addition, its effects on detergency and bacteriostatic abilities are relatively significant. The findings provide sufficient reference data for the further development of  S mukorossi commodities.

Pharmacological and Biological Activities of Different Fractions Methanol Extracts of Gardenia coronaria Buch. -Ham. Leaves

2018 ◽  
Vol 20 (2) ◽  
pp. 139-147
Author(s):  
Abdullah Al Faruq ◽  
Mohammed Ibrahim ◽  
M Mohi Uddin Chowdhury ◽  
Mohiminul Adib ◽  
Mohammad R Haque ◽  
...  
Keyword(s):  
Crude Extract ◽  
Reducing Sugars ◽  
Biological Activities ◽  
Radical Scavenging ◽  
Ethanolic Extract ◽  
Pharmaceutical Journal ◽  
Chloroform Extract ◽  
Zone Of Inhibition ◽  
Ic50 Values ◽  
Dose Dependent

Ethanolic extract and its n-hexane and chloroform soluble fractions of the leaves of Gardenia coronaria Buch. Ham. were screened for their bio-activities. Preliminary phytochemicals screening of crude extract revealed the presence of glycosides, alkaloids, tannins, saponins, reducing sugars and flavonoids in different extracts. In antibacterial test, maximal zone of inhibition obtained against B. cereus (15.3 mm) and in antifungal test maximal zone found against C. albicans (12.7 mm) by the chloroform extract. The crude extract of the plant exhibited notable anti-inflammatory activity. The antioxidant activity was evaluated by DPPH free radical scavenging method where the scavenging activity was concentration dependent with IC50 values of 5.15μg/ml, 8.75μg/ml and 12.71μg/ml for ethanol, nhexane and chloroform extract, respectively. In the castor oil-induced antidiarrheal assay, the crude extract of the plant significantly increased the latency and total count of defecation. Acetic acid-induced writhing reflex due to analgesia was inhibited by 31.18% (by ethanol), 23.67% (by n-hexane) and 24.73% (by chloroform) at 500 mg/kg body wt. in experimental mice. The extractives at doses from 31.25-500 μg/ml, produced inhibition of amylase activity in a dose dependent manner.Bangladesh Pharmaceutical Journal 20(2): 139-147, 2017

Radioprotection of 1,2-dimethylhydrazine-initiated colon cancer in rats using low-dose γ rays by modulating multidrug resistance-1, cytokeratin 20, and β-catenin expression

2015 ◽  
Vol 35 (3) ◽  
pp. 282-292 ◽  
Author(s):  
HM Nabil ◽  
BN Hassan ◽  
AA Tohamy ◽  
HF Waaer ◽  
AE Abdel Moneim
Keyword(s):  
Colon Cancer ◽  
Multidrug Resistance ◽  
Ionizing Radiation ◽  
Tumor Cells ◽  
Low Dose ◽  
Colorectal Tumor ◽  
Cytokeratin 20 ◽  
Γ Irradiation ◽  
Γ Rays ◽  
Γ Ray

Ionizing radiation is a widely used therapy for solid tumors. However, high-dose ionizing radiation causes apoptosis, transforms normal cells into tumor cells, and impairs immune functions, leading to the defects in the removal of damaged or tumor cells. In contrast, low-dose radiation has been reported to exert various beneficial effects in cells. This experimental study investigated the effect of γ rays at low dose on the development of colorectal tumor in a 1,2-dimethylhydrazine (DMH)-induced colon cancer. Colorectal tumor model was induced in Wistar rats by subcutaneous injection of DMH (20 mg/kg) once a week for 15 weeks. Starting from zero day of DMH injection, a single low dose of whole-body γ irradiation of 0.5 Gy/week was applied to the rats. A significant reduction in lipid peroxidation, nitric oxide, and elevation in the glutathione content and antioxidant enzyme activity (superoxide dismutase and catalase) were observed after γ irradiation comparing with DMH group. Moreover, γ ray reduced the expressions of multidrug resistance 1 (MDR1), β-catenin, and cytokeratin 20 (CK20) those increased in DMH-treated rats. However, survivin did not change with γ ray treatment. A histopathological examination of the DMH-injected rats revealed ulcerative colitis, dysplasia, anaplasia, and hyperchromasia. An improvement in the histopathological picture was seen in the colon of rats exposed to γ rays. In conclusion, the present results showed that low-dose γ ray significantly inhibited DMH-induced colon carcinogenesis in rats by modulating CK20, MDR1, and β-catenin expression but not survivin expression.

Changes in structural and optical properties due to γ-irradiation of MgO nanoparticles

2020 ◽  
Vol 108 (4) ◽  
pp. 315-320
Author(s):  
Maryam Amini ◽  
Mohammad Hossein Majles Ara
Keyword(s):  
Optical Properties ◽  
Dose Rate ◽  
Structural Properties ◽  
Gamma Spectroscopy ◽  
Hexagonal Lattice ◽  
Crystal Defects ◽  
Γ Irradiation ◽  
Mgo Nanoparticles ◽  
Before And After ◽  
Γ Ray

AbstractIn this research, the influence of γ-irradiation on the optical and structural properties of magnesium oxide (MgO) nanoparticles was studied. The MgO nanoparticles were irradiated with doses 100 Gy, 1 kGy, 10 kGy and 20 kGy from 60Co source. The as-synthesized samples of MgO nanoparticles prepared by the sol-gel technique were analyzed by XRD which suggested the double phase; cubic and hexagonal structures of the material. The crystal defects that produced in the cubic and hexagonal lattice were studied before and after 60Co γ-irradiation in a gamma cell by different dose rates in order to report the changes in structural properties of the MgO nanoparticles. The irradiated and un-irradiated samples were characterized by XRD and UV–Vis. The XRD pattern of MgO nanoparticles is showed that the crystal size of MgO nanoparticles being increased with increasing the γ-ray dose rate. For optical absorption, the UV–Visible absorption spectra of MgO nanoparticles are showed that when the dose rate is increased, the value of band gap is decreased. Also, the experimental values of the mass attenuation coefficient of MgO nanoparticles have been calculated before and after γ-irradiation by using the gamma spectroscopy method. Therefore, the results are showed that γ-ray irradiation has various effects on structural, morphological and optical properties.

scholarly journals Studies of Biological Activities of the Roots of Bombax ceiba L.

2019 ◽  
Vol 22 (2) ◽  
pp. 219-223
Author(s):  
Md Hasanur Rahman ◽  
Mohammad A Rashid ◽  
Tofail Ahmad Chowdhury
Keyword(s):  
Free Radical ◽  
Crude Extract ◽  
Biological Activities ◽  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Pharmaceutical Journal ◽  
Free Radical Scavenging ◽  
Clot Lysis ◽  
Albino Rat ◽  
Dpph Method

Bioactivities of the methanolic crude extract of root of Bombax ceiba L. and its organic and aqueous soluble partitionates were studied to investigate its medicinal importance. In Free radical scavenging assay by DPPH method, the aqueous soluble partitionate (AQSF) demonstrated the highest free radical scavenging activity with IC50 value of 3.33 ± 0.25 μg/ml. The brine shrimp lethality bioassay of different partitionates of the root demonstrated the significant lethality by the hexane soluble partitionate (HSF) having LC50 value of 1.19 ± 0.10 µg/ml. Among different fractionates of the root, the highest percentage (44.55 ± 0.12%) of clot lysis was exhibited by AQSF. The crude extract revealed promising antidiarrheal, hypoglycemic, central and peripheral analgesic activities at both doses of 200- and 400- mg/kg body weight in Swiss-Albino rat model. Bangladesh Pharmaceutical Journal 22(2): 219-223, 2019

scholarly journals Biological Activities of the Methanolic Extracts of Coccinia indica and Mikania scandens Leaves Available in Bangladesh

2017 ◽  
Vol 16 (1) ◽  
pp. 87-93
Author(s):  
Md Akhtar E Ekram ◽  
Md Enamul Haq Sarker ◽  
Afrin Priya Talukder ◽  
Badhan Sarker ◽  
Md Salah Uddin ◽  
...  
Keyword(s):  
Crude Extract ◽  
Leaf Extract ◽  
Biological Activities ◽  
Radical Scavenging ◽  
Pseudomonas Sp ◽  
Cytotoxic Assay ◽  
Leaf Extracts ◽  
Penicillium Notatum ◽  
Coccinia Indica ◽  
Antimicrobial Assay

Biological activities of the methanolic leaf extracts of Coccinia indica and Mikania scandens were observed through antimicrobial assay, cytotoxic assay and antioxidant activity through DPPH (1,1-diphenyl-2- picrylhydrazyl) radical scavenging assay with a comparison of IC50 values of extracts with standard antioxidant BHT (butylatedhydroxytoluene). In case of crude extract of Coccinia indica, antimicrobial assay showed that Pseudomonas sp., Escherichia coli were susceptible at a dose of 150?g/disc out of five tested bacteria. Again, out of five fungi strains, Phytopthora sp., Penicillium notatum, Aspergillus niger were sensitive against 150 ?g/disc containing crude extract. In the case of Mikania scandens, antimicrobial assay showed that Pseudomonas sp., Rhizobium for Vigna mongu (RVM), Rhizobium for Cicer arietinum (RCA)were susceptible at a dose of 150 ?g/disc, while Escherichia coli was susceptible at only 75 ?g/disc. Furthermore, out of five fungi strains, Phytopthora sp., Penicillium notatum were sensitive against 150?g/disc while Aspergillus niger was sensitive against 100 ?g/disc and 150 ?g/disc of M. scandens crude extract. The DPPH free radical scavenging activity of C. indica leaf extract displayed that it was capable of scavenging the 50% DPPH at the dose of 130 ?g/ml and itindicated that the plant extract had moderate to high antioxidant activity. However, Mikania scandens, the IC50 value was 125?g/ml which indicated that M. scandens leaf extract had strong antioxidant potentialities than the leaf extract of C. indica. Cytotoxic assay showed that the methanolic leaf extracts of C. indica and M. scandens were highly toxic for the aquatic organisms at the concentrations of above 104.60 and 89 ?g/ml, respectively.Dhaka Univ. J. Pharm. Sci. 16(1): 87-93, 2017 (June)

The stability of dislocation networks under various oxygen-doping conditions in superconducting Bi2Sr2CaCu2Oy single crystals and their influence on the flux pinning properties

1994 ◽  
Vol 52 ◽  
pp. 802-803
Author(s):  
Y. Feng ◽  
X. Y. Cai ◽  
R. J. Kelley ◽  
D. C. Larbalestier
Keyword(s):  
Single Crystals ◽  
Oxygen Content ◽  
Basal Plane ◽  
Flux Pinning ◽  
Pinning Centers ◽  
Before And After ◽  
Anomalous Peak ◽  
Basal Plane Dislocation ◽  
The Stability ◽  
Further Development

The issue of strong flux pinning is crucial to the further development of high critical current density Bi-Sr-Ca-Cu-O (BSCCO) superconductors in conductor-like applications, yet the pinning mechanisms are still much debated. Anomalous peaks in the M-H (magnetization vs. magnetic field) loops are commonly observed in Bi2Sr2CaCu2Oy (Bi-2212) single crystals. Oxygen vacancies may be effective flux pinning centers in BSCCO, as has been found in YBCO. However, it has also been proposed that basal-plane dislocation networks also act as effective pinning centers. Yang et al. proposed that the characteristic scale of the basal-plane dislocation networksmay strongly depend on oxygen content and the anomalous peak in the M-H loop at ˜20-30K may be due tothe flux pinning of decoupled two-dimensional pancake vortices by the dislocation networks. In light of this, we have performed an insitu observation on the dislocation networks precisely at the same region before and after annealing in air, vacuumand oxygen, in order to verify whether the dislocation networks change with varying oxygen content Inall cases, we have not found any noticeable changes in dislocation structure, regardless of the drastic changes in Tc and the anomalous magnetization. Therefore, it does not appear that the anomalous peak in the M-H loops is controlled by the basal-plane dislocation networks.

Benefit/Risk Profile of Combined Antiplatelet Therapy with Ticlopidine and Aspirin

1991 ◽  
Vol 65 (05) ◽  
pp. 504-510 ◽  
Author(s):  
Raffaele De Caterina ◽  
Rosa Sicari ◽  
Walter Bernini ◽  
Guido Lazzerini ◽  
Giuliana Buti Strata ◽  
...  
Keyword(s):  
Platelet Function ◽  
Low Dose ◽  
Bleeding Time ◽  
Ex Vivo ◽  
Stable Coronary Artery Disease ◽  
High Dose ◽  
Single Drug ◽  
Before And After ◽  
Serum Thromboxane ◽  
Artery Disease

SummaryTiclopidine (T) and aspirin (ASA) are two antiplatelet drugs both capable of prolonging bleeding time (BT), with a different mechanism of action. A synergism in BT prolongation has been reported and is currently considered an argument for not recommending their combination. However, a profound suppression of platelet function might be a desirable counterpart of a marked prolongation of BT, with a possible use in selected clinical situations. We therefore studied ex vivo platelet function (aggregation by ADP 0.5-1-2.5 μM; adrenaline 0.75-2.5 μM; collagen 1.5-150 μg/ml; arachidonic acid 1 mM; PAF 1 μM; adrenaline 0.17 μM + ADP 0.62 μM; serum thromboxane ([TX]B2 generation) and BT (Mielke) in 6 patients with stable coronary artery disease receiving such combination. Patients underwent sequential laboratory evaluations at baseline, after 7 days of T 250 mg b.i.d., before and after the intravenous administration of ASA 500 mg, respectively, and, finally, after a minimum of 7 days of sole ASA oral administration (50 mg/day). The experimental design, therefore, allowed a comparison of T and ASA effects (2nd and 4th evaluation), and an assessment of the combination effect (3rd evaluation). Platelet aggregation in response to all doses of ADP was depressed more by T than by ASA. Conversely, responses to adrenaline, and arachidonate were affected more by ASA than by T. For all other agents, differences were not significant. T + ASA combination was more effective (p <0.05) than either treatment alone in depressing responses to high-dose collagen (% over control, mean ± SEM: T: 95 ± 3; ASA: 96 ± 5; T + ASA: 89 ± 4). Serum TXB2 (basal, ng/ml: 380 ± 54) did not change with T (372 ± 36), dropped to <1 ng/ml on ASA injection and slightly re-increased to 9.1 ± 3.1 ng/ml on oral low-dose ASA. BT (basal 7.4 ± 0.6 min) was affected similarly by T (9.2 ± 0.8) or ASA (9.7 ± 0.9) alone, but increased to 15.0 ± 0.7 min on combination treatment (106% increase over control). Thus, the strong synergism in BT prolongation by ASA-T combination has a counterpart in the inhibition of platelet function in response to strong stimuli such as high-dose collagen, not otherwise affected significantly by single-drug treatment. This effect is a possible rationale for the clinical evaluation of T + ASA combination.

The Challenges in Dealing with Organized Crime and its Consequences in Modern Societies in Albania, Kosovo and Macedonia – the Balkan Peninsula

2015 ◽  
Vol 5 (1) ◽  
pp. 161
Author(s):  
Bashkim Selmani ◽  
Bekim Maksuti
Keyword(s):  
Organized Crime ◽  
Balkan Peninsula ◽  
Human Mind ◽  
Negative Consequences ◽  
The Public ◽  
Before And After ◽  
History Of ◽  
European Standards ◽  
Organized Crime Groups ◽  
Further Development

The profound changes within the Albanian society, including Albania, Kosovo and Macedonia, before and after they proclaimed independence (in exception of Albania), with the establishment of the parliamentary system resulted in mass spread social negative consequences such as crime, drugs, prostitution, child beggars on the street etc. As a result of these occurred circumstances emerged a substantial need for changes within the legal system in order to meet and achieve the European standards or behaviors and the need for adoption of many laws imported from abroad, but without actually reading the factual situation of the psycho-economic position of the citizens and the consequences of the peoples’ occupations without proper compensation, as a remedy for the victims of war or peace in these countries. The sad truth is that the perpetrators not only weren’t sanctioned, but these regions remained an untouched haven for further development of criminal activities, be it from the public state officials through property privatization or in the private field. The organized crime groups, almost in all cases, are perceived by the human mind as “Mafia” and it is a fact that this cannot be denied easily. The widely spread term “Mafia” is mostly known around the world to define criminal organizations.The Balkan Peninsula is highly involved in these illegal groups of organized crime whose practice of criminal activities is largely extended through the Balkan countries such as Kosovo, Albania, Macedonia, Serbia, Bosnia, Croatia, Montenegro, etc. Many factors contributed to these strategic countries to be part of these types of activities. In general, some of the countries have been affected more specifically, but in all of the abovementioned countries organized crime has affected all areas of life, leaving a black mark in the history of these states.

α-Glucosidase Inhibition, Antioxidant and Docking Studies of Hydroxycoumarins and their Mono and Bis O-alkylated/acetylated Analogs

2018 ◽  
Vol 15 (2) ◽  
pp. 127-135 ◽  
Author(s):  
Parvesh Singh ◽  
Nomandla Ngcoya ◽  
Ramgopal Mopuri ◽  
Nagaraju Kerru ◽  
Neha Manhas ◽  
...  
Keyword(s):  
In Silico ◽  
Biological Activities ◽  
Wide Spectrum ◽  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Catalytic Site ◽  
Docking Simulations ◽  
In Silico Docking ◽  
Anti Oxidant

Background: Diabetes Mellitus (DM) is a complex metabolic disease illustrated by abnormally high levels of plasma glucose or hyperglycaemia. Accordingly, several α-glucosidase inhibitors have been developed for the treatment of diabetes and other degenerative disorders. While, a coumarin ring has the privilege to represent numerous natural and synthetic compounds with a wide spectrum of biological activities e.g. anti-cancer, anti-HIV, anti-viral, anti-malarial, anti-microbial, anti-convulsant, anti-hypertensive properties. Besides this, coumarins have also shown potential to inhibit α-glucosidase leading to a generation of new promising antidiabetic agents. However, the testing of O-substituted coumarins for α-glucosidase inhibition has evaded the attention of medicinal chemists. Methods: For O-alkylation/acetylation reactions, the hydroxyl coumarins (A-B) initially activated by K2CO3 in dry DMF were reacted with variedly substituted haloalkanes at room temperature under nitrogen. The synthesized compounds were tested for their α-glucosidase (from Saccharomyces cerevisiae) inhibitory activity and anti-oxidant activity using DPPH radical scavenging activity. In silico docking simulations were conducted using CDocker module in DS (Accelrys) to explore the binding modes of the representative compounds in the catalytic site of α-glucosidase. Results: All the coumarin analogues (A1, B1, A2-A10, B2-B8) including their precursors (A-B) were evaluated for their in vitro α-glucosidase inhibition using acarbose as a standard inhibitor. All the mono O-alkylated coumarins (except A1) showed significant (p <0.05) α-glucosidase inhibition relative to the hydroxyl coumarin (A) with IC50 values ranging between 11.084±0.117 to 145.24± 29.22 µg/mL. Compound 7-(benzyloxy)-4, 5-dimethyl-2H-chromen-2-one (A9) bearing a benzyl group (Ph-CH2-) at position 7 showed a remarkable (p <0.05) increase in the activity (IC50 = 11.084±0.117 µg/mL), almost four-fold more than acarbose (IC50 = 40.578±5.999 µg/mL). The introduction of –NO2 group dramatically improved the anti-oxidant activity of coumarin, while the O-alkylation/acetylation decreased the activity. Conclusion: The present study describes the synthesis of functionalized coumarins and their evaluation for α-glucosidase inhibition and antioxidant activity under in vitro conditions. Based on IC50 data, the mono O-alkylated coumarins were observed to be stronger inhibitors of α-glucosidase with respect to their bis O-alkylated analogues. Coumarin (A9) bearing O-benzyloxy group displayed the strongest α-glucosidase inhibition, even higher than the standard inhibitor acarbose. The coumarin (A10) bearing –NO2 group showed the highest anti-oxidant activity amongst the synthesized compounds, almost comparable to the ascorbic acid. Finally, in silico docking simulations revealed the role of hydrogen bonding and hydrophobic forces in locking the compounds in catalytic site of α-glucosidase.

Novel Piperazine Amides of Cinnamic Acid Derivatives as Tyrosinase Inhibitors

2018 ◽  
Vol 16 (1) ◽  
pp. 36-44 ◽  
Author(s):  
Zehra Tuğçe Gür ◽  
Fatma Sezer Şenol ◽  
Suhaib Shekfeh ◽  
İlkay Erdoğan Orhan ◽  
Erden Banoğlu ◽  
...  
Keyword(s):  
Cinnamic Acid ◽  
Active Site ◽  
Agaricus Bisporus ◽  
Biological Activities ◽  
Docking Simulation ◽  
Cinnamic Acid Derivatives ◽  
In Silico Docking ◽  
Amide Derivatives ◽  
Tyrosinase Inhibitors ◽  
Further Development

Background: A series of novel cinnamic acid piperazine amide derivatives has been designed and synthesized, and their biological activities were also evaluated as potential tyrosinase inhibitors. Methods: Compounds 9, 11 and 17 showed the most potent biological activity (IC50 = 66.5, 61.1 and 66 &#181;M, respectively). In silico docking simulation was performed to position compound 11 into the Agaricus bisporus mushroom tyrosinase’s active site to determine the putative binding interactions. Results and Conclusion: The results indicated that compound 11 could serve as a promising lead compound for further development of potent tyrosinase inhibitors.

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