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Designed for Florida Association of Code Enforcers, in association with the Florida Institute of Government, this material helps prepare participants for the Report Writing questions on the Code Enforcement certification exam. I have no control over the content of the handouts/workbook used for this training program, so the content is more dry and static than I would like.
Report Writing
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ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
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бейсенбаева альбина+ресторан+идея
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2015 has been an amazing year for Global Witness. I feel enormously proud to work for an organisation that is currently deeply engaged in 19 campaigns across 29 countries–investigating and exposing injustice, and advocating for systemic change to end corruption, conflict, human rights abuse and environmental destruction. The team has had many great campaign successes throughout the year and I wanted to share just a few of them with you: For over 20 years, Global Witness has exposed how many of the world’s worst environmental and human rights abuses are driven by the exploitation of natural resources, and corruption in the global political and economic system. We have only been able to achieve change on these issues because of the generous support of our donors and other supporters. Next year we will continue to work towards a better world: a world where corruption is challenged and accountability prevails, so that all can thrive within the planet’s boundaries and governments act in the public interest.
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ABSTRACT Background:The main objective of the study is to determine the anti-arthritic effect of whole plant ethanolic extract of Polygonum glabrum belonging to the family Polygonaceae in Female wistar rats using the Freund’s Complete Adjuvant (FCA) model . Methods:The plants areal parts were collected near Tirupathi hills, Chittoor district of Andhra Pradesh in India. The Phytoconstituents were identified through the chemical tests. Ethanol (95%) was used to obtain the whole plant extraction through Soxhlet extractor. Female SD rats were used for antiarthritic screening. Arthritis was induced using FCA, and the anti-arthritic effect of the ethanolic extract of P.glabrum was studied at doses of 250 and500 mg/kg. The effects were compared with those of indomethacin (10 mg/kg). At the end of the study, theliver enzyme levels were determined and a radiological examination was carried out. Results and Discussion:The preliminary phytochemical analysis of the ethanolic extract of Polygonum glabrum showed the presence of alkaloids, tannins, flavonoids and saponins. P. glabrum at 250 and 500 mg/kg significantly inhibited the FCA-induced arthritis in the rats. This was manifested by as a decrease in the paw volume. The arthritic control animals exhibited a significant decrease in body weight compared with control animals without arthritis. P. glabrum treated animals showed dose dependent reduction in decrease in body weight and arthritis.At the same time, P.glabrum significantly altered the biochemical and haematological changes induced by FCA (P < 0.05). The anti-arthritic effect of P.glabrum was comparable with that of Indomethacin. Conclusion:The whole plant extract of P.glabrum showed significant anti-arthritic activity against FCA-induced arthritis in female Wistar rats.
Evaluation of anti-arthritic activity of Polygonum glabrum
Evaluation of anti-arthritic activity of Polygonum glabrum
Dr. Raghavendra Kumar Gunda
This presentation uses a 2011 Florida law as a context for examining course modality as a contact zone. The law requires all high-school students to take at least one online course before graduation. The politically minded law ignores complex issues of access and ethics that become reified in our FYC courses. I will examine the “cultural and ideological characteristics” of this technological requirement to identify how writing instruction in various modalities can accommodate (or defend against) student expectations for online learning.
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Background: The main aim of present research investigation is to formulate the Risperidone Fast Dissolving tablets. Risperidone, an atypical antipsychotic, belongs to BCS Class-II and used for treating schizophrenia, bipolar mania and autism by blocking D2 and 5-HT2A receptors. Methods: The Fast Dissolving tablets of Risperidone were prepared employing different concentrations of Crospovidone and Croscarmellose sodium in different combinations as a Superdisintegrants by Direct Compression technique using 32 factorial design. The concentration of Crospovidone and Croscarmellose sodium was selected as independent variables, X1 and X2 respectively whereas, wetting time, Disintegration time, t50% ,t90%were selected as dependent variables. Results and Discussion: Totally nine formulations were designed, preapred and are evaluated for hardness, friability, thickness, Assay, Wetting time, Disintegration time, In-vitro drug release. From the Results concluded that all the formulation were found to be with in the Pharmacopoeial limits and the In-vitro dissolution profiles of all formulations were fitted in to different Kinetic models, the statistical parameters like intercept (a), slope (b) & regression coefficient (r) were calculated. Polynomial equations were developed for Wetting time, Disintegration time, t50%, t90%. Validity of developed polynomial equations were verified by designing 2 check point formulations (C1, C2). According to SUPAC guidelines the formulation (F5) containing combination of 10% Crospovidone and 10% Croscarmellose, is the most similar formulation (similarity factor f2= 93.556, dissimilarity factor f1= 0.976& No significant difference, t= 0.022) to marketed product (RISPERDAL-4). Conclusion: The selected formulation (F5) follows First order, Higuchi’s kinetics, mechanism of drug release was found to be Fickian Diffusion (n= 0.383).
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Designed for Florida Association of Code Enforcers, in association with the Florida Institute of Government, this material helps prepare participants for the Report Writing questions on the Code Enforcement certification exam. I have no control over the content of the handouts/workbook used for this training program, so the content is more dry and static than I would like.
Report Writing
Report Writing
Chris Friend
ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
ጣፋጭ ዜና መጽሄት ቁጥር 4 ቅፅ 2. ቁጥር 2 መጋቢት 2008
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2015 has been an amazing year for Global Witness. I feel enormously proud to work for an organisation that is currently deeply engaged in 19 campaigns across 29 countries–investigating and exposing injustice, and advocating for systemic change to end corruption, conflict, human rights abuse and environmental destruction. The team has had many great campaign successes throughout the year and I wanted to share just a few of them with you: For over 20 years, Global Witness has exposed how many of the world’s worst environmental and human rights abuses are driven by the exploitation of natural resources, and corruption in the global political and economic system. We have only been able to achieve change on these issues because of the generous support of our donors and other supporters. Next year we will continue to work towards a better world: a world where corruption is challenged and accountability prevails, so that all can thrive within the planet’s boundaries and governments act in the public interest.
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ABSTRACT Background:The main objective of the study is to determine the anti-arthritic effect of whole plant ethanolic extract of Polygonum glabrum belonging to the family Polygonaceae in Female wistar rats using the Freund’s Complete Adjuvant (FCA) model . Methods:The plants areal parts were collected near Tirupathi hills, Chittoor district of Andhra Pradesh in India. The Phytoconstituents were identified through the chemical tests. Ethanol (95%) was used to obtain the whole plant extraction through Soxhlet extractor. Female SD rats were used for antiarthritic screening. Arthritis was induced using FCA, and the anti-arthritic effect of the ethanolic extract of P.glabrum was studied at doses of 250 and500 mg/kg. The effects were compared with those of indomethacin (10 mg/kg). At the end of the study, theliver enzyme levels were determined and a radiological examination was carried out. Results and Discussion:The preliminary phytochemical analysis of the ethanolic extract of Polygonum glabrum showed the presence of alkaloids, tannins, flavonoids and saponins. P. glabrum at 250 and 500 mg/kg significantly inhibited the FCA-induced arthritis in the rats. This was manifested by as a decrease in the paw volume. The arthritic control animals exhibited a significant decrease in body weight compared with control animals without arthritis. P. glabrum treated animals showed dose dependent reduction in decrease in body weight and arthritis.At the same time, P.glabrum significantly altered the biochemical and haematological changes induced by FCA (P < 0.05). The anti-arthritic effect of P.glabrum was comparable with that of Indomethacin. Conclusion:The whole plant extract of P.glabrum showed significant anti-arthritic activity against FCA-induced arthritis in female Wistar rats.
Evaluation of anti-arthritic activity of Polygonum glabrum
Evaluation of anti-arthritic activity of Polygonum glabrum
Dr. Raghavendra Kumar Gunda
This presentation uses a 2011 Florida law as a context for examining course modality as a contact zone. The law requires all high-school students to take at least one online course before graduation. The politically minded law ignores complex issues of access and ethics that become reified in our FYC courses. I will examine the “cultural and ideological characteristics” of this technological requirement to identify how writing instruction in various modalities can accommodate (or defend against) student expectations for online learning.
Modality as Contact Zone: The Convolution of Access, Politics, and Ethics in ...
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Chris Friend
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Project lanjutan database bioskop
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Background: The main aim of present research investigation is to formulate the Risperidone Fast Dissolving tablets. Risperidone, an atypical antipsychotic, belongs to BCS Class-II and used for treating schizophrenia, bipolar mania and autism by blocking D2 and 5-HT2A receptors. Methods: The Fast Dissolving tablets of Risperidone were prepared employing different concentrations of Crospovidone and Croscarmellose sodium in different combinations as a Superdisintegrants by Direct Compression technique using 32 factorial design. The concentration of Crospovidone and Croscarmellose sodium was selected as independent variables, X1 and X2 respectively whereas, wetting time, Disintegration time, t50% ,t90%were selected as dependent variables. Results and Discussion: Totally nine formulations were designed, preapred and are evaluated for hardness, friability, thickness, Assay, Wetting time, Disintegration time, In-vitro drug release. From the Results concluded that all the formulation were found to be with in the Pharmacopoeial limits and the In-vitro dissolution profiles of all formulations were fitted in to different Kinetic models, the statistical parameters like intercept (a), slope (b) & regression coefficient (r) were calculated. Polynomial equations were developed for Wetting time, Disintegration time, t50%, t90%. Validity of developed polynomial equations were verified by designing 2 check point formulations (C1, C2). According to SUPAC guidelines the formulation (F5) containing combination of 10% Crospovidone and 10% Croscarmellose, is the most similar formulation (similarity factor f2= 93.556, dissimilarity factor f1= 0.976& No significant difference, t= 0.022) to marketed product (RISPERDAL-4). Conclusion: The selected formulation (F5) follows First order, Higuchi’s kinetics, mechanism of drug release was found to be Fickian Diffusion (n= 0.383).
Formulation Development and Evaluation of Risperidone Fast Dissolving Tablets
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