Monday, March 29, 2021

Applications of Paper Chromatography in Pharmaceutical Analysis

Paper chromatography is one of the kinds of chromatography which is used for separating complex mixtures and identifying the analytes or components. The mixture gets separated since several analytes will attract more to the stationary phase (a piece of specialized paper) and several components can be attracted to the mobile phase hence they travel with it. Paper chromatography is typically utilized as an instructing to explain the basic functions of chromatography, however it is used in some pharmaceutical applications, let's check it out.
  • Reaction monitoring.
  • To ensure the control of the purity of pharmaceuticals.
  • For the study of ripening and fermentation.
  • For the analysis of the reaction mix in biochemical laboratories.
  • To detect contaminated substances in beverages and foodstuffs.
  • For the analysis of cosmetics.
  • Separation and purification techniques for components.
  • Forensic testing.
  • Performance-enhancing drug testing.

 It is the one of the oldest method used in several applications of chemistry. Let’s check some common applications of paper chromatography.

  • Paper chromatography is specifically used to separate mixtures of polar and non-polar molecules.
  • As it has a broad range of mobile phase or solvent system, it is used to identify unknown organic and inorganic components from sample mixtures.
  • Colored mixtures, such as pigments, are separated and identified using paper chromatography as a qualitative technique.
  • Sugar, nucleic acids, lipids, amino acids and some biomolecules can be easily detected using paper chromatography by spraying with sufficient reagents on stationary phase (e.g. Ninhydrin solution).
  • In the pharma field it is used for the determination of drugs, hormones etc.
  • It can be used in forensics testing and drug abuse, by comparing an unknown chromatogram with a known chromatogram which may aid in the investigation of a crime scene.
  • Paper chromatography can be used to analyze the fermentation and ripening process.

Commonly asked questions on paper chromatography are as follows.

What industries use paper chromatography?
Paper chromatography is commonly used in the analysis of various foods as well as in the pharmaceutical industries. It is mostly used in the analysis of colors that is used in the ice-creams, sweets, jams & jellies, beverages, and other foodstuffs.

What is the principle of paper chromatography?
The paper chromatography and thin-layer chromatography (TLC) works on the same principle that is partition chromatography in which the molecules are partitioned or distributed between liquid phases.

What factors affect paper chromatography?
Many factors affect paper chromatography such as the concentration of the sample, the length of the paper, type of solvent or mobile phase used, the thickness of paper, quality of paper used, and working temperature.

 

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Applications of HPTLC in Pharmaceutical Analysis
Applications of Thin Layer Chromatography in Pharmaceutical Analysis
Advantages and Disadvantages of Column Chromatography
What is the basic principle of HPTLC
what are the advantages of TLC over HPLC chromatography
Advantages and disadvantages of mass spectrometry
Advantages and disadvantages of ion-pair chromatography
Advantages and Disadvantages of Thin Layer Chromatography
Advantages and Disadvantages of UV Visible Spectroscopy
 

Saturday, March 27, 2021

Monophasic and biphasic liquid dosage forms

Monophasic and biphasic dosage are types of liquid dosage forms used for oral, external, special, and parenteral administration. However, there are some advantages, applications, and differences between monophasic and biphasic liquid dosage forms, so let's take a look at them.

Medication is more effective when they reach their site of action hence different dosage forms and routes are used to treat the various diseases. The dosage form is the medium that delivered medication to their sites of action within the body. It is a pharmaceutical product that contains a combination of drugs and excipients, formulated in a particular configuration and apportioned into a specific dose. Pharmaceutical dosage forms are classified as solid dosage form, semi-solid dosage form, liquid dosage form, and gaseous dosage form based on their physical form.
Liquid dosage forms are pourable pharmaceutical formulations that contain a mixture of active pharmaceutical ingredients (API) and excipients dissolved or suspended in an appropriate solvent or mixture of solvents. It is intended to provide a maximum therapeutic effect to patients who have trouble swallowing oral solid dosage forms.

Monophasic liquid dosage forms:

The monophasic dosage form is a single-phase system consisting of two or more components. It is the simple form of presenting the medication for rapid and high absorption of the drug. This is represented by the true solution and the true solution is a clear homogeneous mixture prepared by dissolving the solute in an appropriate solvent. The component of a solution that is present in large quantities is called "SOLVENT," while the component that is present in small quantities is called "SOLUTE."

Classification of monophasic liquid dosage forms:

Monophasic liquid dosage forms for oral use: example- linctuses, mixtures, syrups, elixirs, drops, and draughts, etc.
Monophasic liquid dosage forms for a particular use: example- nasal drops, ear drops, eye drops, eye lotions, mouthwashes, aerosols, gargles, inhalations, and throat paints, etc.
Monophasic liquid dosage forms for external use: example-lotions and liniments etc.
Parenteral solutions: example- intravenous, subcutaneous, and intramuscular injections, etc.

Advantages of monophasic liquid dosage forms:

  • It rapidly absorbs the drug than solid dosage form since the drug is already in the form of a solution.
  • Because it is homogeneous, it provides a more consistent dose than suspension or emulsion, which requires shaking.
  • It can be administered by various routes such as oral, parenteral, otic, ophthalmic, and nasal.
  • As compared with solid dosage forms (tablets, capsules) it is easy to swallow, especially for children and old patients.
  • The unpleasant taste and smell of the drug are masked by adding sweeteners and flavor-enhancing agents.

Disadvantages of monophasic liquid dosage forms:

  • It may undergo hydrolysis if exposed to direct sunlight, so it needs to be store in a cool and dark place.
  • The stability of the drug is reduced by hydrolysis or oxidation.
  • Water is used in the formulation as a vehicle that is susceptible to microscopic growth; as a result, a preservative is required.

Biphasic liquid dosage forms:

It is a liquid dosage form is one that has two phases; suspensions and emulsions are two examples of biphasic liquid dosage forms. A biphasic system consists of a solid dispersed state and a liquid continuous phase that can be aqueous or oily and is stabilized by the addition of a suspended agent. These are commonly taken orally or through the parenteral route, and they are also used for external applications.
It is used when the drugs are poorly soluble in the solvent. Drugs can be either liquid or solid from the dispersed phase of the system, when the solid drug is distributed in the dispersion medium; the formed system is called a suspension. When the liquid drug is delivered into the dispersion medium, the system form is called emulsion.

Classification of biphasic liquid dosage forms:

The biphasic liquid dosage forms have two types, emulsion and suspension.
Emulsion dosage form: It is a thermodynamically unstable system consisting of two immiscible liquid phases, one of which is dispersed as globules within the other and stabilized by an emulsifying agent. It has two types, water in oil type (w/o), and oil in a water type (o/w). Examples-application, liniment, and lotion, etc.
Suspension dosage form: It is a biphasic liquid or semi-solid dosage form, in which insoluble solid particles of the drug are homogeneously dispersed in a liquid or semi-solid medium. Examples- Gels, lotion, aerosols, inhalation, and eye drop, etc.

Advantages of biphasic liquid dosage forms:

  • It is used for the drugs that are insoluble in solution; therefore it is necessary to prepare an insoluble form of the drug, which is then administered as a suspension.
  • It exhibits higher bioavailability rates than other dosage forms.
  • Suspension can offer prolonged action of the drug since solid particles must be dissolved before absorption.
  • Two incompatible ingredients/drugs can be included in a dose, one in each phase of the emulsion.

Disadvantages of biphasic liquid dosage forms:

  • Not all drugs are compatible to formulate with biphasic form.
  • It is bulky and therefore difficult to handle, transport and store.
  • It is costly compared with the solid dosage form.

Difference between monophasic and biphasic liquid dosage form:

Liquid oral doses comprise a wide range of dosage forms, broadly classified as the monophasic and biphasic liquid dosage forms. The major difference between monophasic and biphasic liquid dosage forms is that the monophasic liquid dosage forms have a single homogeneous phase, whereas biphasic liquid dosage forms consist of two distinct phases. Both forms include at least one drug in formulation, monophasic forms are homogeneous and completely dissolve in liquid, whereas biphasic forms are not dissolved in a vehicle.

Commonly asked questions on dosage forms are as follows.

What is the classification of dosage forms?
Pharmaceutical dosage forms are classified based on physical form and route of administration, based on the physical form are solid, semi-solid, liquid, and gaseous dosage form.

How many types of emulsions are there?
There are two basic types of emulsions, oil in a water type (o/w) and, water in an oil type (w/o).

How many types of suspension are there in the pharmacy?
Based on the ratio of solids, suspension dosage forms are empirically classified as dilute or concentrated systems and based on the nature and behavior of solids, suspensions are classified as flocculated or deflocculated.
 
 

Saturday, March 20, 2021

Difference between sustained and controlled release dosage form

The major difference between sustained and controlled release dosage forms is that in sustained medication the dose is maintained over a long period and the release of the drug is not fixed per unit time, however, in controlled forms, the release of the drug is very definite per unit time. Whereas, in controlled drug delivery drug is delivered locally or systematically at a predetermined rate for a specified time.

The drug is effective only when it arrives at the site of action therefore a variety of dosage forms and routes of administration are used to deliver the drug. The dosage form of a pharmaceutical product refers to its method of entering or delivering a biological system. The dosage forms are classified according to the physical form and route of administration.
According to physical form, the dosage forms are classifieds into solid dosage forms, semisolid, liquid, and gaseous dosage forms. According to the route of drug administration, the dosage forms are classifieds into oral, parenteral (injection), inhalation, topical, sublingual, rectal, nasal, buccal, and transdermal routes administration, etc.

Sustained release dosage form:

The purpose of sustained-release dosage forms is to release drugs at a predetermined rate so that a constant concentration of drugs is maintained for a specific time, according to the needs of the body throughout the treatment period.
The major advantage of developing sustained-release formulations is to modify and increase the performance of drug by increasing the time of drug action, reduce the frequency of dosing, reducing side effects, reducing the required dose employed, and providing the shortest possible time using the smallest amount of medication administered by the most appropriate route.

Controlled release dosage form:

Controlled drug delivery is that which delivers the active pharmaceutical ingredients (API) systematically or locally at a predetermined rate for a prescribed time. The controlled release drug delivery system employs drug encapsulating devices that allow for the controlled release of the drug over longer periods, which can range from days to months.
Controlled-release systems provide a sustained-release profile as well, but unlike sustained-release drug delivery systems, they are formulated or designed to produce predictable constant concentrations of active pharmaceutical ingredient (API), independently of the biological environment of the application site. This means that, unlike the sustained-release system, they are controlling the concentration of an active ingredient in the target tissue or blood, not just the release of the drug from the dosage form.

Here are some of the points of difference between sustained and controlled release dosage forms are mentioned.
  • sustained release dosage forms follow first-order kinetics, while controlled release dosage forms have followed zero-order kinetics.
  • In sustained release implies a slow release of the medication over a period of time and this release may or may not be controlled, Whereas the controlled release is a completely zero-order release, the medication releases over time irrespective of concentration.
  • sustained-release medication is restricted to oral dosage forms whereas controlled-release medications are used in a variety of administration routes, such as oral vaginal, and transdermal administration, etc.
  • In sustained release forms, the dosage is maintained for a long time and drug release is not definite per unit time, while drug release is predictable very definite per unit time in controlled-release forms.
Commonly asked questions on dosage forms are as follows.

What are the types of modified release dosage forms?
A variety of modified dosage forms are designed by pharmaceutical industries to reduce side effects as well as increase patient compliance by reducing the frequency of dosing. The classification of a modified release dosage form is sustained-release, prolonged-action, extended-release, targeted-release, delayed-release, repeat-action, and controlled-release dosage forms.

What is the importance of dosage forms?
Appropriate dosage forms are required to protect the drug from destructive influences of the atmospheric conditions such as moisture or oxygen, to deliver extended action of the drug through a control release mechanism to mask the unpleasant taste and odor, and to protect the drug from being destroyed from gastric acid of oral administration, etc.

What are the types of pharmaceutical tablets?
Different types of tablets in pharmacy are formulated and they can vary in size, shape, weight, hardness, thickness, dissolution, and disintegration. Compressed tablets, film-coated tablets, enteric-coated tablets, chewable tablets, sugar-coated tablets, effervescent tablets, buccal and sublingual tablets are some of the types of tablets.
 
 

Thursday, March 18, 2021

Difference between Dissolution and Solubility

The major difference between dissolution and solubility is that the dissolution is a kinetic process, by which a solute in a solid, liquid, or gaseous phase dissolves in a solvent to form a solution, Whereas solubility is the maximum concentration of a solute that can dissolve in a solvent at a specified temperature, it is a thermodynamic process.

Dissolution and solubility are related to each other, yet there is a slight disparity amongst them. Dissolution is the procedure as solute dissolves up in medium (solvent), but solubility is the outcome of dissolution. In this process, the solid part refers to the solute, and the liquid is referred to as a solvent, several factors affect this type of reaction such as temperature, solute size, and solvent properties.
Before understanding the difference between dissolution and solubility it is important to know the three essential components involved in the term dissolution and solubility i.e. solvent, solute, and solution.
Solute: A solute is a compound that dissolves in a solvent.
Solvent: A solvent is a liquid that is used to dissolve a solute.
Solution: The mixture formed when a solute is dissolved in a solvent is referred to as a solution.
Solutes may be liquids, solids, or gas, and although solvents are usually liquids, they can also be solid and gaseous solvents.
Difference between dissolution and solubility

Below are some points of differences between dissolution and solubility are mentioned.
  • Dissolution is the capacity of solute to be dissolved whereas solubility is the rate of solute dissolving in a solution.
  • Dissolution is a kinetic process whereas solubility is a thermodynamic process.
  • In dissolution, solute dissolves in a solvent to form a solution whereas solubility is the outcome of dissolution.
  • Dissolution is measured in mol/s whereas solubility is measured in mol/kg.

Dissolution:

Dissolution is a kinetic process that is performed by the dissolution test apparatus (USP, IP, BP dissolution apparatus) for the oral solid dosage form and is used to find the rate of a solute dissolving in a solution, in which the process the solutes are always soluble in the medium or solvent.
Factors affecting dissolution:
  • Surface area
  • Physicochemical properties of the drug
  • The temperature of the process
  • The concentration of the solute
  • Viscosity and polarity of the solvent

Solubility:

Solubility is a thermodynamic process in which the chemical property refers to the ability of a particular solute, the substance, to liquefy in the solution or solvent. Solubility is used for finding out the solute capacity to be dissolved in a particular solvent quantity, in which the process solutes are not always soluble in the medium or solvent it depends on the solute properties.
Factors affecting solubility:
  • The concentration of the solute
  • The temperature of the system
  • The polarity of the solvent
  • The polarity of the solute
  • The pressure of the system
Commonly asked questions on solubility and dissolution are as follows.

How does solubility affect dissolution rate?
Both solubility and dissolution rate are two different phenomena. The solubility of the sample in a solvent may be poor, but its dissolution rate might be high. A solute, on the other hand, can be very soluble but take a long time to reach its final saturation concentration.

What is the advantage of dissolution testing?
The dissolution can determine the rate of release and the extent of absorption of the dosage forms, which is a major advantage of dissolution.

What is dissolution in chemistry?
A mechanism by which a solute in a liquid, solid, or gaseous phase dissolves in a solvent to form a solution is known as dissolution.


Wednesday, March 17, 2021

Difference between emulsion and suspension

The major difference between emulsion and suspension is that the suspension is a heterogeneous mixture in which the dispersed particles are large and settle on standing, whereas the emulsion is a heterogeneous mixture of two immiscible liquids in which the dispersed particles do not settle on standing.

Suspensions:

The pharmaceutical suspension is a biphasic liquid or semi-solid dosage form, in which insoluble solid drug particles are homogeneously dispersed in a liquid or semi-solid medium. The internal phase is uniformly distributed in the external phase, resulting in a coarse dispersion. The internal phase is ranging in size from 0.5 to 5 m, while the external phase, which is generally aqueous in some instances, can be an organic or oily liquid for non-oral use.
The pharmaceutical suspensions are classified into four major parts according to their pharmaceutical use i.e. oral suspensions, parenteral suspensions, ophthalmic suspensions and, suspensions for external use.
  • A suspension is a heterogeneous mixture of large dispersed particles that settle upon standing.
  • The size of suspended particles more than 1000 nm, and is visible to the naked eye.
  • It can scatter light or opaque.
  • For the stability of the formulation, suspending agents are needed.
  • Both orally and topically applications are also possible with compounded suspensions.
  • Freezing should be avoided during storage as it will lead to aggregation.
  • Suspension dosage forms are also opaque when mixed but on standing, it's clear and separate.
  • It can be filtered out.
  • Solid particles are dispersed in any medium, which can be solid, liquid, or gas.

Emulsions:

The pharmaceutical emulsion is a thermodynamically unstable system that consists of two immiscible liquid phases, one of which is dispersed as globules within the other and is stabilized by a third substance known as an emulsifying agent. An example of an emulsion is oil and water they are immiscible and when mixed and shaken form emulsions.
Pharmaceutical emulsions are classified into two types 1. Oil in a water type (o/w), 2. Water in oil type (w/o).
  • An emulsion is a heterogeneous mixture of two immiscible liquids and a type of colloid and dispersed particles, which do not settle upon standing.
  • The dispersed particles range in size from 1 to 1000 nm and are invisible to naked eyes.
  • It can show the Tyndall effect
  • For the stability of the formulation, emulsifying agents are needed.
  • Topical and oral applications are also possible with compounded emulsions.
  • Freezing should be avoided during storage as it leads to cracking.
  • Emulsion dosage forms are opaque in appearance.
  • It cannot be filtered out.
  • The dispersed medium and dispersed phase in the emulsion are both liquids.
Difference between emulsion and suspension

Here are points are mentioned to understand the differences between suspension and emulsion.
  • Two substances in any phase of matter, such as solid, liquid, or gas, can be contained in a suspension, whereas an emulsion consists of only two immiscible liquids.
  • In emulsification, only stabilization is possible where you can make the emulsion more stable by using an emulsifier.
  • To increase product stability, emulsifying agents are required for emulsion, while suspending agents are required for suspension.
  • Suspensions are simple to separate, while emulsions may or may not be, it is depending on the state of matter in which particles are present in either of them.
Commonly asked questions on dosage forms are as follows.

What are the types of liquid dosage forms?
The liquid dosage forms are divided into two types based on phase: monophasic liquid dosage form and biphasic liquid dosage form. Some examples of liquid dosage forms are liniments, lotions, solution, draughts, syrups, linctuses, creams, mixtures, drops, mouthwashes, douches, elixirs, and eye drops, etc.

Is milk an emulsion or suspension?
Since the fat globules in milk are suspended in water, milk is oil in water emulsion.

What are the different routes of drug administration?
A route of administration is the path by which medication is taken into the body. Oral, enteral, parenteral (injection), topical, rectal, ocular, otic, sublingual, and buccal are some of the routes of drug administration.

Sunday, March 14, 2021

Different Types of Conductometric Titration

Learn the different types of conductometric titration

Conductivity measures the ability of the solution to transport the electrical current, adding an element to the solution (Base) is the process of conductometric titration. Change in conductivity or ions which change the concentration of substances. for example, the solution conductivity decreases if the hydrochloric acid (HCL) is titrated with sodium hydroxide (NaOH), It happens on the basis that the fast-moving ions are replaced by ions which move slow.

Principle of the conductometric titration:
Throughout a process of titration, an ion is replaced with another and the difference in ionic conductivities of these ions directly affects the overall electrolytic conductivity of the solution.

Applications of conductometric titration:
  • It is used to check water pollution
  • It is used to determine the salinity of the seawater
  • It is used to determine the alkalinity of the freshwater
  • Conductometry is used in quantitative analysis of the compound
  • Used to tracing microorganisms in foodstuff.
The type of conductive titration is mentioned as follows.
  • Acid-base titration
  • Precipitation titration
  • Replacement titration
  • Redox titration (oxidation-reduction)
  • Complexometric titration
Types of Conductometric Titration
Acid-base titration:
By neutralizing acid or base with the known concentration of an acid or base, an acid-base titration may be used to determine the unknown concentration of an acid or base.
Precipitation titration:
The forms of titration that include the formation of precipitate throughout the titration technique are known as precipitation titrations. In precipitation titration, the titrant reacts with the analyte to form insoluble material known as a precipitate.
Replacement titration:
The replacement titration is used when the direct or back titration does not produce a sharp endpoint of the analysis. It is mainly used to titrate oxalates, benzoates, and phosphates, etc.
Redox titration:
Redox titration is the most commonly used laboratory method for identifying the concentration of unknown analytes and it depends on an oxidation-reduction reaction among the analyte and titrant.
Complexometric titration:
Complexometric titration is a type of volumetric analysis in which a colored complex is a formation to indicate the endpoint of a titration. Complexometric titrations are particularly applicable to determine the metal ions in the sample solution.


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Difference between gas chromatography and liquid chromatography

The major difference between gas and liquid chromatography is that gas chromatography uses gas as a mobile phase (nitrogen or helium), while liquid chromatography uses is a liquid (methanol or acetonitrile), which can be either polar or non-polar solvent.

Chromatography is the most commonly used method for the separation of analytes in chemical laboratories for isolation, purification, and analysis as well as in the chemical or pharmaceutical process industry as a part of small and large-scale development. The sample is separated into two components such that the mobile phase is either liquid or gas, and the stationary phase is either solid or liquid.
Some of the most common forms of chromatography are high-performance liquid chromatography, gas chromatography, thin-layer chromatography (TLC or HPTLC), ion-exchange chromatography, and column chromatography.
Difference between gas chromatography and liquid chromatography

The key differences between gas chromatography and liquid chromatography are below.
Gas chromatography:
GC is one more extensively used chromatography technique of separation. In this technique the mobile phase is generally a passive gas such as nitrogen, helium or argon which is also known as a carrier gas, the columns are made up with inert materials, packed and capillary columns are used to separate the sample components which are volatile. Capillary columns offer more resolution and are relatively expensive than the other columns.
  • Mobile phase in GC is a gas.
  • Separation is mainly based on the analytes boiling points.
  • Analysis can be done in only in the column.
  • Gaseous and volatile compounds can be applied in the separation.
  • Due to high temperatures, some components may be degrading.
  • Separation of components depends on the boiling point, so it is not very flexible in case of separation optimization.
  • The analysis is fast and usually measured in minutes.
  • Provide better resolution.
  • Solvents that vaporize can be used.
Liquid chromatography:
Liquid chromatography is the most popular technique for separation of the sample mixture on the basis of the interaction between the molecules in the sample with mobile phases and stationary phase. It can be either in a column or on the sheet with a mobile phase and solid support in the form of a stationary phase.
The mobile phase chromatography travels through the stationary phase to bring with different sample components. Interactions between chromatography medium and sample molecules can depend on many factors such as hydrophobicity size, affinity, and charge. Liquid chromatography technology is a sophisticated form which uses pressure with help of the pump, to separate the analyte by the column, is called high-performance liquid chromatography (HPLC). It is now the widely used methods of pharmaceutical analysis for quantitative and qualitative analysis.
  • Liquid mobile phase is used in LC.
  • Separation of analytes depends on the interaction of the solute with the stationary phase.
  • Separation can be done in column or sheet.
  • Any soluble compound can separate by LC.
  • Generally done at room temperature so that the heat-sensitive compounds can be analyzed safely and no degradation occurs between analyze.
  • LC is a relatively time-consuming technique.
  • Generally gives a higher or broad peak, which results in less resolution.
  • Polar solvents used in LC (water, methanol).

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Advantages and disadvantages of suppositories dosage form

 Learn the various advantages and disadvantages of the suppositories dosage form.

Medications are effective only when they reach their site of action, so different dosage forms, as well as different routes of drug administration, are used to deliver the drug to the body. Dosage forms are pharmaceutical products that are particular mixtures of drug and excipients; they are needed to deliver an accurate dose to the target tissue, protect the active pharmaceutical ingredient, and mask the taste and odor of the drug. Depending on the physical form, dosage forms can classify into solid, semi-solid, liquid, and gaseous forms. Depending on the route of administration, dosage forms can be classified into oral, parenteral, topical, inhalation, and rectal routes of administration.

The suppository is a solid dosage form containing one or more active ingredients and is used to deliver the medication in the body cavities such as the rectum/vagina. It dissolves and melts on-site and produces a local action or systemic absorption of the active ingredients. It may melt at body temperature or dissolved or dispersed on a suitable basis that may be soluble or dispersible in water.

There are two types of suppository base lipophilic and hydrophilic suppository. Lipophilic suppositories are fat and wax-based which can be melted according to the human body. The hydrophilic suppository is glycerin-based and requires liquid for dissolution.

Advantages of suppositories dosage form:

  • The major advantage of the suppository dosage form is that the drug is rapidly absorbed through the mucous membranes by delivers directly into body cavities.
  • It is a convenient route of administration for drugs that cause vomiting, irritate the GIT, and drugs that are destroyed at the acidic pH of the stomach.
  • The suppositories dosage form is useful when oral therapy is restricted or oral administration is not possible.
  • It is suitable for unconscious patients, uncooperative patients, and patients suffering from severe vomiting.
  • It provides rapid onset of action as compared to the oral route because the absorption of the drug through rectal mucosa directly reaches blood (avoids the first-pass metabolism).
  • Prolonged drug action can be achieved using suppositories dosage form.
  • It does not have systemic side effects compared to other dosage forms.
  • Total bioavailability can be achieved compared to oral dosage forms.
  • Compared to the parenteral drug administration it does not have pain or a site of action-related issues.
  • It does not need to be swallowed like tablets, capsules, caplets and powders, emulsions, suspensions, syrups, mixtures, drops, linctus, and allergens that cause vomiting or irritation.
  • The rectal route of administration offers a much more constant atmosphere for the drug to be absorbed than the oral route.
  • No issue of drugs with unpleasant taste and odor, since they do not need to be swallowing.

Disadvantages of suppositories dosage form:

  • The major disadvantage of the suppository dosage form is that most patients feel uncomfortable taking the drug through the body cavity, so it is not used as broadly as oral dosage forms.
  • Children and elderly patients hesitate to take medication and have difficulty taking self-medication.
  • Some types of suppositories require special storage conditions such as refrigerators to prevent the base from being liquefied.
  • The suppository manufacturing process is difficult compared with oral solid dosage forms.
  • Suppositories are not suitable as a dosage form for drugs that irritate the mucous membrane.
  • Diseases such as diarrhea can affect the absorption of drugs.

Commonly asked questions on dosage forms are as follows.

What are the types of suppositories?
The classification of suppositories is rectal suppositories, vaginal suppositories (pessaries), urethral suppositories (bougies), nasal suppositories, ear suppositories.

What are the advantages of suppositories over tablets dosage form?
The major advantages of suppositories over a tablet are provided topical and systemic effects, improved medication bioavailability, reduced the first-pass metabolism, and accommodates patients who have difficulty swallowing pills.

How many types of capsules are there?
Hard gelatin capsules and soft gelatin capsules are the two types of capsules available which are depending on the physical state of the medication to be filled. They come in a numeral of sizes and shapes, and they can contain one or more active ingredients.
 
 

Difference between tablets and capsules

The major difference between tablets and capsules is that the tablet is prepared by compressing solids such as granules and powders, and the capsule consists of solids or semi-solids, or oily drugs enclosed in a dissolvable gelatin container.

The active pharmaceutical ingredients (API) are only effective when they reach their site of action and hence according to the physical form of the medication (dosage forms) different routes of drug administration are used.

Capsules and tablets most commonly prescribed oral dosage form by doctors. Both are two different forms of medicine that we take when we are sick. The tablet is known as the most commonly used oral pharmaceutical dosage. Commonly, the compression process is used to manufacture a solid dose of the tablet. About two-thirds of all medicines given to a patient by doctors are solid doses, and half of them are the tablets.

To encapsulate drugs, we use a shell or a container called a capsule. A capsule is a two-part shell container, which is soft and hard-shell and is usually made of gelatin. Capsules are odorless and tasteless and are easy to swallow for patients, especially for children. The major advantage of capsules is that they can be easy to swallow.

The another major difference between a tablet and a capsule is that the tablet is a kind of medicine that we can cut in two or crush it, while we have to swallow the capsule without cutting it because it cannot crush or cut.

Difference between tablets and capsules

Depending on the administration, appearance, production process, advantages and disadvantages, some points of differences between tablets and capsules are as follows.
  • Tablets can be prepared with various shapes and sizes. The capsule comes with a specific size and shape.
  • A tablet contains compressed powder in solid form. A capsule contains powder or jelly which is enclosed in a gelatin shell.
  • Sometimes the tablet is difficult to swallow, especially the larger tablet. The capsules are considered easy to swallow.
  • The tablets are inexpensive because its manufacturing process is simple. The capsules are expensive because their manufacturing process is less complex than the tablets.
  • Tablets have more potential than capsules. Capsules have less potential than tablets.
  • The tablet is usually taken orally, sublingually, intra-vaginally, and rectally. The capsule is usually administered orally.
  • The tablets can be used as a continuous-release as it can be coated with sugar or similar substances that mean the drug will not immediately enter the bloodstream. But, normally the capsule is entered directly into the bloodstream.
  • The tablets have a longer shelf life and keep their potential for a long time as compared with capsules.
  • Gelatin shell can protect the medicine from light, moisture, and air, which is not possible in tablets.
  • The tablets are formulated with a limited number of drugs and excipients but in capsules, many drugs and ingredients are mixed.
  • Tablets can only be prepared with solids such as powders, but in capsules, we can fill gel or semi-solid materials.
  • The tablet needs to be coated with a sweetening material to protect it from taste and smell, but the capsule does not need to be coated, as the shell does not have taste and smell.
  • The capsule is easily digested easily and quickly, as compared with tablets.

Tablets vs Capsules
Various shapes and sizes < >Specific shapes and sizes
                Compressed powder in solid form < > Powder or jelly enclosed in a gelatin shell
More potential < > Less potential
    Formulated with a limited drugs < > Formulated with number of drugs
      Prepared only with solids < > Can fill gel or semi-solids      


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Saturday, March 13, 2021

Factors affecting conductivity

Ohm's law can be defined as the conductivity easily by the V= IR, Where V the voltage there in the sample, I the current, and R are the resistance.  Conduct determines the ability of the material to conduct the electricity.
Factors affecting conductivity
Factors affecting the conductivity measurements are mentioned as follows.
Size of the ions:
If the size of the ion increases the conductivity also increases, due to its inversely proportional to the size of the ions.
The concentration of the sample solution:
When the concentration of sample solution increases, the conductance can be decreased due to it is inversely proportional to the conductivity; therefore the conductivity measurement requires a diluted sample solution.
Nature of electrolyte:
Strong electrolytes totally dissociate into ions, consequently, the conductance of the solutions have high.
Number ions present in the sample solution:
It generally depends on the dissolution of the sample in ions. The quantity of ions in solution is specifically relative to the conductance.
Temperature:
The conductivity of the electrolyte increases when the temperature rises. This is due to ion mobility by raise the temperature.
The charge of the ions: