CONNECTION APPROACHES BETWEEN TRADITIONAL AND MODERN PHARMACOLOGICAL PROFILE OF SHOREA ROBUSTA GAERTN. F.: A REVIEW

Shorea robusta is regarded as an important medicine in Ayurveda. S. robusta Gaertn. f. belongs to family Dipterocarpaceae, and traditionally, it is used to treat wounds, ulcers, leprosy, cough, gonorrhea, earache, and headache and many more. The use of different parts of this plant such as leaves, resin, and bark as a medicament for the treatment of various conditions is well documented in literature. It is the rich source of flavonoids, saponins, steroids, tannins, phenols, etc. mainly triterpenoids, which play the prominent role for their therapeutic potential in the drug. These compounds are believed to be responsible for the pharmacological activities of plant extract. The present review clarified the main active ingredients and pharmacological effects of S. robusta as a promising plant as a result of effectiveness and safety. Further studies should be carried out this plant to discover the unrevealed part of it which may serve for the welfare of humankind

PRODUCT RECALL: A COMMENTARY ON RISING INCIDENCES

There has been an increasing trend in the number of prescribed and over-the-counter drug recall over the last few years. The recall is usually due to company’s discovery, customer’s complaint or Food and Drug Administration (FDA) observation. The process of recall involves a planned specific course of action, which addresses the depth of recall, need for public warning, and the extent of effectiveness checks for the recall. The FDA review and/or recommend changes to the firm’s recall strategy, as appropriate. The critical recall information list includes the identity of the product; summary of the failure; amount of product produced in the distribution chain and direct account. Product recalls clashes thousands of companies every year affecting: sales, testing customer relationships and disrupting supply chains. Drug recall is incubus for pharmaceutical companies. It effects the reputation of the company. The reason for the recall can be divided into two categories: manufacturing related and safety/efficacy related. It is essential to follow all the guidelines related to drug development and manufacturing procedure to minimize drug recall. Peer Review History: Article received on- 19 October,    Revised on- 26 December,   Accepted on- 30 December, Available online 15 January 2017 Academic Editor: Ahmad Najib, Universitas Muslim Indonesia,  Indonesia, [email protected] UJPR follows the most transparent and toughest ‘Advanced OPEN peer review’ system. The identity of the authors and, reviewers will be known to each other. This transparent process will help to eradicate any possible malicious/purposeful interference by any person (publishing staff, reviewer, editor, author, etc) during peer review. As a result of this unique system, all reviewers will get their due recognition and respect, once their names are published in the papers. We expect that, by publishing peer review reports with published papers, will be helpful to many authors for drafting their article according to the specifications. Auhors will remove any error of their article and they will improve their article(s) according to the previous reports displayed with published article(s). The main purpose of it is ‘to improve the quality of a candidate manuscript’. Our reviewers check the ‘strength and weakness of a manuscript honestly’. There will increase in the perfection, and transparency. Received file:        Reviewer's Comments: Average Peer review marks at initial stage: 6.5/10 Average Peer review marks at publication stage: 8.0/10 Reviewer(s) detail: Dr. Luisetto Mauro, AUSL PC, Piacenza Area,  Italy, [email protected] Dr. Mahmoud S. Abdallah, University of Sadat city, Egypt, [email protected] Similar Articles: RISING INCIDENCES OF PRODUCT RECAL

RISING INCIDENCES OF PRODUCT RECALL

There has been an increasing trend in the number of prescribed and over-the-counter drug recall over the last few years. The recall is usually due to company’s discovery, customer’s complaint or Food and Drug Administration (FDA) observation. The process of recall involves a planned specific course of action, which addresses the depth of recall, need for public warning, and the extent of effectiveness checks for the recall. Product recalls clashes thousands of companies every year affecting: sales, testing customer relationships and disrupting supply chains. Drug recall is incubus for pharmaceutical companies. It effects the reputation of the company. The reason for the recall can be divided into two categories: manufacturing related and safety/efficacy related. It is essential to follow all the guidelines related to drug development and manufacturing procedure so as to minimize drug recall.         Peer Review History: Article received on- 4 September; Revised on- 12 October; Accepted on- 16 October 2016, Available online 15 November 2016 Academic Editor: Ahmad Najib, Universitas Muslim Indonesia,  Indonesia, [email protected] UJPR follows the most transparent and toughest ‘Advanced OPEN peer review’ system. The identity of the authors and, reviewers will be known to each other. This transparent process will help to eradicate any possible malicious/purposeful interference by any person (publishing staff, reviewer, editor, author, etc) during peer review. As a result of this unique system, all reviewers will get their due recognition and respect, once their names are published in the papers. We expect that, by publishing peer review reports with published papers, will be helpful to many authors for drafting their article according to the specifications. Auhors will remove any error of their article and they will improve their article(s) according to the previous reports displayed with published article(s). The main purpose of it is ‘to improve the quality of a candidate manuscript’. Our reviewers check the ‘strength and weakness of a manuscript honestly’. There will increase in the perfection, and transparency. Received file:        Reviewer's Comments: Average Peer review marks at initial stage: 6.5/10 Average Peer review marks at publication stage: 7.5/10 Reviewer(s) detail: Dr. Maha Khalifa Ahmed Khalifa, Al-Azhar Universit - Cairo, Egypt, [email protected] Dr. Mohamed Derbali, Faculty of Pharmacy, Monastir, Tunisia, [email protected] Similar Articles: PRODUCT RECALL: A COMMENTARY ON RISING INCIDENCE

A comparative study of the relationship between the recovery of movement and the anatomical alignment in fractures around the elbow

Background: The injury around the elbow joint is a common condition in any age group, especially in children as a result of fall, during the course of a child's normal play. The aim of the present study was to study the relationship between the recovery of movements and the anatomical alignment in fractures around the elbow.Methods: In the present study, 110 cases of fractures around elbow were included. The treatment with conservative or operative procedure depends on the surgeon concerned and his priorities. Sixty-six cases were treated conservatively, and 56 cases required operative intervention. At the time of follow up examination, cases were assessed as to the anatomical and functional point of view according to Flynn's criteria. We evaluated the reduction as per alignment in anteroposterior axis, lateral axis, and angulation. The patients were followed up for over 24 months.Results: Patients who had good anatomical alignment (grade A) showed 96.87% satisfactory result as compared to the patient who had fair anatomical alignment (91.66%) and poor anatomical alignment (54.54%). Thus in grade A where alignment was up to 76 points, we had satisfactory result in 96.87% patients, where as in grade C where alignment was less than 50 points, the result in 45.5% of patients was poor.Conclusions: Patients who had good anatomical alignment achieved, showed higher recovery of movement compared to the patient who had fair anatomical alignment and poor anatomical alignment

Photo-damage to Keratinocytes by Quinine Photosensitization under mild Ultraviolet-B Exposure

Simultaneous and sufficient exposure to sunlight and drug cause phototoxic reactions in the skin. In the present study, the photosensitizing activity of quinine (Q) was studied. Evidences obtained by reduction of cell viability, mitochondrial damage, DNA damage, ROS generation, lysosome damage and phosphatidyl serine translocation as a marker of apoptosis indicates that exposure of quinine treated keratinocytes to UV-B radiation results in quinine photosensitization and subsequent reactions which alter normal cellular processes. Quinine absorbs strongly in UV-B region (330 nm). It reduced viability of cells significantly as observed through MTT assay. Reduction of cell viability was confirmed through accumulation of Rhodamine 123 dye which showed that quinine and UV-B treated cells accumulate less than control cells confirmed that mitochondrial membrane potential was disturbed. Increased intracellular ROS production was measured through DCF fluorescence. Early apoptosis was confirmed through phosphatidyl serine translocation in the membrane. Increased lysosome damage was observed through acridine orange accumulation in the lysosmes. Single stranded damage was confirmed through comet assay and apoptosis was confirmed through EB/AO staining.  These results show that UV-B radiation elicits phototoxic effects in keratinocytes through reactive oxygen species generation

A REVIEW ON LEARNING AND MEMORY

Learning is defined as the acquisition of information and skills and subsequent retention of the information is called memory. Dementia is one of the ages related mental problems and characteristic symptom of various neurodegenerative disorders including Alzheimer’s disease which is age related. It is a progressive and neurodegenerative disorder. The analysis of the anatomical and physical bases of learning and memory is one of the great successes of modern neuroscience. The action of drugs on memory is more or less specific and serious depending on the memory system affected. So the present study is therefore focused on the various types of learning and memory. Key Words: Learning, Memory, Dementia

Bottom-Up and Top-Down Approaches for MgO

In this chapter, we present an overview of synthesis of MgO nanoparticles and thin films by using top-down and bottom-up approaches. The bottom-up approaches are generally utilized to grow nanoparticles by the methods that involve chemical reactions. Sometimes, methods based on these reactions are also able to grow thin films. The top-down approaches are preferred for growing thin films where bulk material is used for depositions. The methods, which are frequently used, are radio frequency sputtering, pulsed lased deposition, and molecular beam epitaxy and e-beam evaporation. Sometimes, methods like mechanical milling and high energy ball milling are used to grow nanoparticles

Sustainable green approach to synthesize Fe 3 O 4 /α-Fe 2 O 3 nanocomposite using waste pulp of Syzygium cumini and its application in functional stability of microbial cellulases

Synthesis of nanomaterials following green routes have drawn much attention in recent years due to the low cost, easy and eco-friendly approaches involved therein. Therefore, the current study is focused towards the synthesis of Fe(3)O(4)/α-Fe(2)O(3) nanocomposite using waste pulp of Jamun (Syzygium cumini) and iron nitrate as the precursor of iron in an eco-friendly way. The synthesized Fe(3)O(4)/α-Fe(2)O(3) nanocomposite has been extensively characterized through numerous techniques to explore the physicochemical properties, including X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, Ultraviolet-Vis spectroscopy, field emission scanning electron microscope, high resolution transmission electron microscope and vibrating sample magnetometer. Further, efficiency of the Fe(3)O(4)/α-Fe(2)O(3) nanocomposite has been evaluated to improve the incubation temperature, thermal/pH stability of the crude cellulase enzymes obtained from the lab isolate fungal strain Cladosporium cladosporioides NS2 via solid state fermentation. It is found that the presence of 0.5% Fe(3)O(4)/α-Fe(2)O(3) nanocomposite showed optimum incubation temperature and thermal stability in the long temperature range of 50–60 °C for 15 h along with improved pH stability in the range of pH 3.5–6.0. The presented study may have potential application in bioconversion of waste biomass at high temperature and broad pH range

Quality by Design: A new practice for production of pharmaceutical products

This is the advanced approach for development of pharmaceutical product with full range and specified limits of variables during procurements, storage and manufacturing process with a qualification, at desired level of quality within the limits of low and higher values of variables to ensures  the Pharmaceutical product Quality by design (QbD) of manufacturing a finished product. The Quality by Design is depicted and a portion of its components recognized and process parameters with quality characteristics are identified for every unit activity. Advantages, openings and steps engaged with Quality by Design of Pharmaceutical items are depicted. The point of the pharmaceutical advancement is to plan a quality item and it’s assembling procedure to reliably convey the proposed execution of the item. Quality can't be tried into items however quality ought to be worked in by outline. It incorporates the Quality target item profile, basic quality traits and key parts of Quality by Design. It likewise gives correlation between item quality by end item testing and item quality by Quality by Design. The establishment of Quality by Design is ICH Guidelines. It depends on the ICH Guidelines Q8 for pharmaceutical improvement, Q9 for quality hazard administration, Q10 for pharmaceutical quality frameworks. It moreover gives utilization of Quality by Design in pharmaceutical improvement and assembling of pharmaceuticals. Keywords: Quality by Design, Design Space, Target Product Quality Profile, Critical Quality Attribute