際際滷shows by User: shinganaarti / http://www.slideshare.net/images/logo.gif 際際滷shows by User: shinganaarti / Fri, 26 Feb 2021 08:04:38 GMT 際際滷Share feed for 際際滷shows by User: shinganaarti Acid and base buffer /slideshow/acid-and-base-buffer/243469025 acidandbase-buffer-210226080439
Acids and bases buffers ARRHENIUS CONCEPT THE LEWIS CONCEPT-THE ELECTRON DONOR ACCEPTOR SYSTEM BRONSTED-LOWRY CONCEPT (PROTON TRANSFER THEORY buffer action ph scale buffer capacity acid base balance isotonicity method isotonic soltions buffer solutions in pharmaceutical preparations ]]>

Acids and bases buffers ARRHENIUS CONCEPT THE LEWIS CONCEPT-THE ELECTRON DONOR ACCEPTOR SYSTEM BRONSTED-LOWRY CONCEPT (PROTON TRANSFER THEORY buffer action ph scale buffer capacity acid base balance isotonicity method isotonic soltions buffer solutions in pharmaceutical preparations ]]>
Fri, 26 Feb 2021 08:04:38 GMT /slideshow/acid-and-base-buffer/243469025 shinganaarti@slideshare.net(shinganaarti) Acid and base buffer shinganaarti Acids and bases buffers ARRHENIUS CONCEPT THE LEWIS CONCEPT-THE ELECTRON DONOR ACCEPTOR SYSTEM BRONSTED-LOWRY CONCEPT (PROTON TRANSFER THEORY buffer action ph scale buffer capacity acid base balance isotonicity method isotonic soltions buffer solutions in pharmaceutical preparations <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/acidandbase-buffer-210226080439-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Acids and bases buffers ARRHENIUS CONCEPT THE LEWIS CONCEPT-THE ELECTRON DONOR ACCEPTOR SYSTEM BRONSTED-LOWRY CONCEPT (PROTON TRANSFER THEORY buffer action ph scale buffer capacity acid base balance isotonicity method isotonic soltions buffer solutions in pharmaceutical preparations
Acid and base buffer from shinganaarti
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Pharmacopoeia /slideshow/pharmacopoeia-242406902/242406902 pharmacopoeia-210208074810
WHAT IS PHARMACOPOEIA? TYPES OF PHARMACOPOEIA HISTORY OF PHARMACOPOEIA CONTENT OF PHARMACOPOEIA WHAT IS MONOGRAPH? PURPOSE OF MONOGRAPH TYPES OF MONOGRAPH IMPORTANCE OF CONTENT OF MONOGRAPH MONOGRAPH DEVELOPMENT PROCESS]]>

WHAT IS PHARMACOPOEIA? TYPES OF PHARMACOPOEIA HISTORY OF PHARMACOPOEIA CONTENT OF PHARMACOPOEIA WHAT IS MONOGRAPH? PURPOSE OF MONOGRAPH TYPES OF MONOGRAPH IMPORTANCE OF CONTENT OF MONOGRAPH MONOGRAPH DEVELOPMENT PROCESS]]>
Mon, 08 Feb 2021 07:48:09 GMT /slideshow/pharmacopoeia-242406902/242406902 shinganaarti@slideshare.net(shinganaarti) Pharmacopoeia shinganaarti WHAT IS PHARMACOPOEIA? TYPES OF PHARMACOPOEIA HISTORY OF PHARMACOPOEIA CONTENT OF PHARMACOPOEIA WHAT IS MONOGRAPH? PURPOSE OF MONOGRAPH TYPES OF MONOGRAPH IMPORTANCE OF CONTENT OF MONOGRAPH MONOGRAPH DEVELOPMENT PROCESS <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/pharmacopoeia-210208074810-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> WHAT IS PHARMACOPOEIA? TYPES OF PHARMACOPOEIA HISTORY OF PHARMACOPOEIA CONTENT OF PHARMACOPOEIA WHAT IS MONOGRAPH? PURPOSE OF MONOGRAPH TYPES OF MONOGRAPH IMPORTANCE OF CONTENT OF MONOGRAPH MONOGRAPH DEVELOPMENT PROCESS
Pharmacopoeia from shinganaarti
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Nomenclature /slideshow/nomenclature-242207722/242207722 nomenclature-210203101242
Nomenclature of organic compounds IUPAC nomenclature classification of organic compound ]]>

Nomenclature of organic compounds IUPAC nomenclature classification of organic compound ]]>
Wed, 03 Feb 2021 10:12:42 GMT /slideshow/nomenclature-242207722/242207722 shinganaarti@slideshare.net(shinganaarti) Nomenclature shinganaarti Nomenclature of organic compounds IUPAC nomenclature classification of organic compound <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/nomenclature-210203101242-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Nomenclature of organic compounds IUPAC nomenclature classification of organic compound
Nomenclature from shinganaarti
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Limit test /slideshow/limit-test-242207563/242207563 limittest-210203100922
Limit test Limit test of Chloride Limit test of Sulphate Limit test of Iron Limit test of Lead Limit test of Heavy Metals ]]>

Limit test Limit test of Chloride Limit test of Sulphate Limit test of Iron Limit test of Lead Limit test of Heavy Metals ]]>
Wed, 03 Feb 2021 10:09:22 GMT /slideshow/limit-test-242207563/242207563 shinganaarti@slideshare.net(shinganaarti) Limit test shinganaarti Limit test Limit test of Chloride Limit test of Sulphate Limit test of Iron Limit test of Lead Limit test of Heavy Metals <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/limittest-210203100922-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Limit test Limit test of Chloride Limit test of Sulphate Limit test of Iron Limit test of Lead Limit test of Heavy Metals
Limit test from shinganaarti
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Impurites /slideshow/impurites/242207094 impurites-210203100128
Definition of Impurity Types of Impurities Sources of Impurity foreign unwanted matter present in a compound which are differ from the actual molecular formula. According to ICH An impurity in a drug of the new drug substance that is not the substance. Chemically a compound is impure if it contains undesirable foreign matter i.e. impurities. Thus chemical purity is freedom from foreign matter Impurities can have unwanted pharmacological or toxicological effect that seriously impact product quality and patient safety. The International Conference on Harmonization (ICH) has formulated a workable guideline regarding the control of impurities. Impurities in pharmaceutical are the unwanted chemicals that remains with the active pharmaceutical ingredient (APIs), or develop during formulation or upon aging of both API and formulated APIs to medicine. The presence of the unwanted chemicals, even in small amount , may influence the efficacy and safety of pharmaceutical product ]]>

Definition of Impurity Types of Impurities Sources of Impurity foreign unwanted matter present in a compound which are differ from the actual molecular formula. According to ICH An impurity in a drug of the new drug substance that is not the substance. Chemically a compound is impure if it contains undesirable foreign matter i.e. impurities. Thus chemical purity is freedom from foreign matter Impurities can have unwanted pharmacological or toxicological effect that seriously impact product quality and patient safety. The International Conference on Harmonization (ICH) has formulated a workable guideline regarding the control of impurities. Impurities in pharmaceutical are the unwanted chemicals that remains with the active pharmaceutical ingredient (APIs), or develop during formulation or upon aging of both API and formulated APIs to medicine. The presence of the unwanted chemicals, even in small amount , may influence the efficacy and safety of pharmaceutical product ]]>
Wed, 03 Feb 2021 10:01:24 GMT /slideshow/impurites/242207094 shinganaarti@slideshare.net(shinganaarti) Impurites shinganaarti Definition of Impurity Types of Impurities Sources of Impurity foreign unwanted matter present in a compound which are differ from the actual molecular formula. According to ICH An impurity in a drug of the new drug substance that is not the substance. Chemically a compound is impure if it contains undesirable foreign matter i.e. impurities. Thus chemical purity is freedom from foreign matter Impurities can have unwanted pharmacological or toxicological effect that seriously impact product quality and patient safety. The International Conference on Harmonization (ICH) has formulated a workable guideline regarding the control of impurities. Impurities in pharmaceutical are the unwanted chemicals that remains with the active pharmaceutical ingredient (APIs), or develop during formulation or upon aging of both API and formulated APIs to medicine. The presence of the unwanted chemicals, even in small amount , may influence the efficacy and safety of pharmaceutical product <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/impurites-210203100128-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Definition of Impurity Types of Impurities Sources of Impurity foreign unwanted matter present in a compound which are differ from the actual molecular formula. According to ICH An impurity in a drug of the new drug substance that is not the substance. Chemically a compound is impure if it contains undesirable foreign matter i.e. impurities. Thus chemical purity is freedom from foreign matter Impurities can have unwanted pharmacological or toxicological effect that seriously impact product quality and patient safety. The International Conference on Harmonization (ICH) has formulated a workable guideline regarding the control of impurities. Impurities in pharmaceutical are the unwanted chemicals that remains with the active pharmaceutical ingredient (APIs), or develop during formulation or upon aging of both API and formulated APIs to medicine. The presence of the unwanted chemicals, even in small amount , may influence the efficacy and safety of pharmaceutical product
Impurites from shinganaarti
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Recrysatlization /slideshow/recrysatlization/242206805 recrysatlization-210203095442
Recrystallization is the most convenient method for purifying organic compounds that are solids at room temperature. Compounds obtained from natural sources, or from reaction mixtures, almost always contain impurities. The impurities may include some combination of insoluble, soluble, and colored impurities. To obtain a pure compound these impurities must be removed. Each type of impurity is removed in a separate step in the recrystallization procedure.]]>

Recrystallization is the most convenient method for purifying organic compounds that are solids at room temperature. Compounds obtained from natural sources, or from reaction mixtures, almost always contain impurities. The impurities may include some combination of insoluble, soluble, and colored impurities. To obtain a pure compound these impurities must be removed. Each type of impurity is removed in a separate step in the recrystallization procedure.]]>
Wed, 03 Feb 2021 09:54:42 GMT /slideshow/recrysatlization/242206805 shinganaarti@slideshare.net(shinganaarti) Recrysatlization shinganaarti Recrystallization is the most convenient method for purifying organic compounds that are solids at room temperature. Compounds obtained from natural sources, or from reaction mixtures, almost always contain impurities. The impurities may include some combination of insoluble, soluble, and colored impurities. To obtain a pure compound these impurities must be removed. Each type of impurity is removed in a separate step in the recrystallization procedure. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/recrysatlization-210203095442-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Recrystallization is the most convenient method for purifying organic compounds that are solids at room temperature. Compounds obtained from natural sources, or from reaction mixtures, almost always contain impurities. The impurities may include some combination of insoluble, soluble, and colored impurities. To obtain a pure compound these impurities must be removed. Each type of impurity is removed in a separate step in the recrystallization procedure.
Recrysatlization from shinganaarti
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Introduction to pharmacology /slideshow/introduction-to-pharmacology-241493073/241493073 introductiontopharmacology-210118093109
introduction to pharmacology, scope of pharmacology, routes of administration of drugs.]]>

introduction to pharmacology, scope of pharmacology, routes of administration of drugs.]]>
Mon, 18 Jan 2021 09:31:09 GMT /slideshow/introduction-to-pharmacology-241493073/241493073 shinganaarti@slideshare.net(shinganaarti) Introduction to pharmacology shinganaarti introduction to pharmacology, scope of pharmacology, routes of administration of drugs. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/introductiontopharmacology-210118093109-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> introduction to pharmacology, scope of pharmacology, routes of administration of drugs.
Introduction to pharmacology from shinganaarti
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Protecting group /slideshow/protecting-group/233803411 protectinggroup-200513123156
A protecting group or protective group is introduced into a molecule by chemical modification of a functional group ]]>

A protecting group or protective group is introduced into a molecule by chemical modification of a functional group ]]>
Wed, 13 May 2020 12:31:56 GMT /slideshow/protecting-group/233803411 shinganaarti@slideshare.net(shinganaarti) Protecting group shinganaarti A protecting group or protective group is introduced into a molecule by chemical modification of a functional group <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/protectinggroup-200513123156-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> A protecting group or protective group is introduced into a molecule by chemical modification of a functional group
Protecting group from shinganaarti
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Cox inhibitor /slideshow/cox-inhibitor-233802363/233802363 coxinhibitor-200513121609
cyclooxygenase inhibitors, topic of medicinal chemistry]]>

cyclooxygenase inhibitors, topic of medicinal chemistry]]>
Wed, 13 May 2020 12:16:09 GMT /slideshow/cox-inhibitor-233802363/233802363 shinganaarti@slideshare.net(shinganaarti) Cox inhibitor shinganaarti cyclooxygenase inhibitors, topic of medicinal chemistry <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/coxinhibitor-200513121609-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> cyclooxygenase inhibitors, topic of medicinal chemistry
Cox inhibitor from shinganaarti
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