Pharmaceutical Tablets - Formulation Quiz
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Questions and Answers

What is the main purpose of adding a binding agent to the tablet mixture?

  • To ensure proper compression of the tablet (correct)
  • To avoid over wetting of the tablet
  • To increase the disintegration time
  • To enhance the color of the tablet

Which step is essential for preparing tablets that are moisture-sensitive?

  • Slugging (correct)
  • Tray drying
  • Tablet screening
  • Direct compression

What characteristic should tablets possess to be considered well-made?

  • Should be larger than a standard size
  • Should be free from defects (correct)
  • Should dissolve in water quickly
  • Should have uniform color

Why is tray drying commonly used in tablet granulation?

<p>It allows for better control of moisture content (C)</p> Signup and view all the answers

What happens if the powder is not wetted properly during granulation?

<p>Granules will be too soft (A)</p> Signup and view all the answers

What is the main role of a lubricant in tablet preparation?

<p>To prevent clumping and ensure smooth filling (B)</p> Signup and view all the answers

What is the significance of the mesh size used during screening of granules?

<p>It influences the size of the granules (C)</p> Signup and view all the answers

When is direct compression preferred in tablet formulation?

<p>When the drug is less than 25% of the total weight (B)</p> Signup and view all the answers

What is the primary reason for including a binder agent in lozenge tablets?

<p>To slow the release of active ingredients. (B)</p> Signup and view all the answers

Which of the following should NOT be added to lozenge tablets?

<p>Disintegrating agents. (C)</p> Signup and view all the answers

What is the characteristic reaction of effervescent tablets when mixed with water?

<p>They liberate carbon dioxide. (D)</p> Signup and view all the answers

Which type of tablet is specifically shaped to ease insertion?

<p>Vaginal tablet. (B)</p> Signup and view all the answers

What is the primary purpose of using disintegrants in tablet formulation?

<p>To aid in breaking the tablet in the gastrointestinal tract. (C)</p> Signup and view all the answers

What is the intended duration of release for implantation tablets?

<p>3-6 months. (C)</p> Signup and view all the answers

What is the role of diluents in tablet preparation?

<p>To increase the bulk for easier compression. (D)</p> Signup and view all the answers

What type of agent must be included in effervescent tablets for their desired effect?

<p>Disintegrating agent. (D)</p> Signup and view all the answers

Which of the following preparations is most suitable for maintaining higher stability of a drug?

<p>Solid preparations (B)</p> Signup and view all the answers

What is one method to reduce the risk of hydrolysis in drugs?

<p>Adding hygroscopic agents (B)</p> Signup and view all the answers

Which of the following agents is used to prevent oxidation in drug formulations?

<p>Oxybenzone (D)</p> Signup and view all the answers

Which condition primarily enhances the rate of polymerization in drug formulations?

<p>Presence of impurities (B)</p> Signup and view all the answers

Which of the following alterations describes optical isomerization?

<p>Changing the compound from one stereoisomer to another (C)</p> Signup and view all the answers

What is a common group that may break down through hydrolysis?

<p>Esters (B)</p> Signup and view all the answers

What effect does lowering the temperature have on polymerization reactions?

<p>Slows down the polymerization process (B)</p> Signup and view all the answers

Which method will NOT help in preventing oxidation of sensitive drugs?

<p>Adding high amounts of water (B)</p> Signup and view all the answers

What effect does probenecid have on indomethacin concentrations in plasma?

<p>It increases indomethacin concentrations. (B)</p> Signup and view all the answers

Which combination of drugs may lead to increased cardiac toxicity due to hypokalemia?

<p>Digoxin and furosemide (A)</p> Signup and view all the answers

Which of the following drug combinations could potentially lead to serious respiratory depression?

<p>Phenobarbitone and alcohol (A)</p> Signup and view all the answers

What is the primary reason for the incompatibility between tetracycline and penicillin?

<p>Tetracycline and erythromycin are incompatible with bactericidal antibiotics. (A)</p> Signup and view all the answers

Why should warfarin and vitamin K not be used together?

<p>They act against each other in the blood coagulation process. (D)</p> Signup and view all the answers

What adverse effect could result from combining glibenclamide with a syrup containing a high percentage of sugar?

<p>Increased blood glucose levels (B)</p> Signup and view all the answers

What is a common side effect of indomethacin that should be considered in its prescription?

<p>Gastric ulcer formation (B)</p> Signup and view all the answers

Which scenario describes physical incompatibility in pharmaceutical mixtures?

<p>Presence of color change in a mixed solution. (D)</p> Signup and view all the answers

What is the acceptable range of active ingredient concentration in tablets according to BP?

<p>90-110% (B)</p> Signup and view all the answers

Which type of tablet coating is primarily used to mask unpleasant taste and protect ingredients from decomposition?

<p>Sugar coating (A)</p> Signup and view all the answers

Which of the following coatings is designed to dissolve in the intestine rather than the stomach?

<p>Enteric coating (B)</p> Signup and view all the answers

What is the primary difference between pastilles and lozenges?

<p>Pastilles dissolve rapidly, while lozenges dissolve slowly. (D)</p> Signup and view all the answers

What classification of drug incompatibility occurs due to antagonistic drug interactions?

<p>Therapeutic incompatibility (C)</p> Signup and view all the answers

Which agents are commonly used in enteric coatings?

<p>Waxes and MC (D)</p> Signup and view all the answers

What is the main purpose of film coating on tablets?

<p>Mask unpleasant taste (A)</p> Signup and view all the answers

Which example represents a common use for lozenges?

<p>Strep sills - lemocin (A)</p> Signup and view all the answers

What effect do drugs like metoclopramide have on gastrointestinal motility?

<p>They increase gastrointestinal motility. (A)</p> Signup and view all the answers

How does paraffin oil affect the absorption of Vitamin A?

<p>It decreases the absorption of Vitamin A. (B)</p> Signup and view all the answers

Which drug combination will likely increase the toxicity of phenylbutazone?

<p>Aspirin and Phenylbutazone (A)</p> Signup and view all the answers

Which of the following drug classes is known to induce liver enzymes and decrease plasma concentration of certain drugs?

<p>Barbiturates (B)</p> Signup and view all the answers

What is the consequence of administering acidic drugs in an acidic media?

<p>Their elimination is reduced. (C)</p> Signup and view all the answers

Which of the following drug combinations might compete for elimination and increase the toxicity of one of the drugs?

<p>Sulfonamide and NaHCO3 (B)</p> Signup and view all the answers

Which of the following substances is an example of a drug that inhibits liver enzymes?

<p>Alcohol (ethanol) (A)</p> Signup and view all the answers

What effect does amphetamine have on gastrointestinal motility?

<p>It decreases gastrointestinal motility. (D)</p> Signup and view all the answers

What is a common cause of picking during tablet compression?

<p>Presence of scratches on punches (D)</p> Signup and view all the answers

Which method can help prevent capping in tablet production?

<p>Using chromium plated punches (D)</p> Signup and view all the answers

What factor can lead to weight variation in tablets?

<p>Inconsistent mixing of lubricants (A)</p> Signup and view all the answers

Lamination in tablets is primarily caused by which of the following?

<p>Air entrapment during compression (A)</p> Signup and view all the answers

Which of the following is a potential solution to address mottling in tablets?

<p>Improving color distribution (C)</p> Signup and view all the answers

What type of punch is recommended to avoid sticking during tableting?

<p>Chromium plated punches (B)</p> Signup and view all the answers

What causes hardiness variation in tablets?

<p>Inconsistent punch pressure (B)</p> Signup and view all the answers

Which processing issue is specifically due to the presence of excess fine powder in granules?

<p>Lamination (D)</p> Signup and view all the answers

What is a primary benefit of using the direct compression method in tablet formulation?

<p>It reduces the need for binding agents. (B)</p> Signup and view all the answers

Which of the following is NOT considered a defect in tablet production?

<p>Uniformity in size (A)</p> Signup and view all the answers

What role do excipients like diluents play in tablet formulation?

<p>They serve as a carrier or vehicle for the active drug. (D)</p> Signup and view all the answers

When is slugging particularly used in tablet manufacturing?

<p>When the ingredients are highly sensitive to moisture. (B)</p> Signup and view all the answers

Which type of compression machine may be utilized for tablet production?

<p>Either single or multiple stations (B)</p> Signup and view all the answers

What can occur if there is an over-wetting of the tablet mixture?

<p>Tablets will be prone to breaking during lubrication. (B)</p> Signup and view all the answers

Which factor is critical for ensuring the proper filling of the die cavity during tablet formation?

<p>Amount of lubricant added (C)</p> Signup and view all the answers

In the context of tablet preparation, what is the significance of the sieve's mesh size?

<p>It influences the size of granules before compression. (A)</p> Signup and view all the answers

Which of the following methods is NOT commonly used for tablet preparation?

<p>Hot melting method (B)</p> Signup and view all the answers

What is a common tablet defect related to appearance?

<p>Mottling (D)</p> Signup and view all the answers

What role do glidants play in tablet formulation?

<p>Enhance flowability (C)</p> Signup and view all the answers

Which of the following is an example of a disintegrant?

<p>Maize starch (B)</p> Signup and view all the answers

What defect in tablet formation is primarily caused by insufficient lubrication?

<p>Sticking (C)</p> Signup and view all the answers

Which excipient is used to mask the bitter taste of a drug?

<p>Sweetening agent (B)</p> Signup and view all the answers

Which type of compression machinery is typically used for producing tablets?

<p>Rotary tablet press (C)</p> Signup and view all the answers

Which of the following substances can act as an anti-adhesive in tablet formulation?

<p>Talc (A)</p> Signup and view all the answers

Flashcards

Lozenges

Tablets designed to dissolve slowly in the mouth, providing a sustained effect on the throat. They typically contain binders to delay the release of the active ingredient.

Effervescent Tablets

Tablets used to prepare a solution by reacting with water. They contain sodium bicarbonate and citric acid (or tartaric acid), which release carbon dioxide upon contact with water, causing effervescence.

Vaginal Tablets

Tablets designed for insertion into the vagina. They are typically oval or almond-shaped for easier insertion.

Implantation Tablets

Small tablets implanted under the skin for prolonged drug delivery, typically lasting 3-6 months.

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Diluents

Substances added to tablets to increase their bulk and make them easier to compress. Examples include lactose, starch, and mannitol.

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Binders

Substances added to tablets to bind the powder particles together and ensure tablet cohesiveness. They can be added in dry or wet form.

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Disintegrants

Substances added to tablets that help them break down in the gastrointestinal tract (GIT). They can work by swelling or reacting with moisture to create effervescence.

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Tablet Compression

The process of compressing powdered ingredients together to form tablets. It involves various excipients like diluents, binders, disintegrants, and lubricants.

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Sugar Coating (Dragification)

A tablet coating that uses sugar, gum, talc, and starch to mask taste, enhance appearance, and protect active ingredients from degradation.

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Film Coating

A tablet coating that uses film-forming agents like CMC, PEG, or carbowax to provide a smooth, thin coating. It's similar to sugar coating but thinner.

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Compression Coating

A tablet coating where dry granules are compressed around a pre-compressed core, without using solvents.

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Enteric Coating

A tablet coating designed to resist stomach acid and release the drug in the intestines. This is used for drugs that are sensitive to stomach acid, irritate the stomach, or need to be absorbed in the intestines.

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Therapeutic Incompatibility

The incompatibility that occurs when two or more ingredients in a prescription have opposing therapeutic effects.

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Chemical Incompatibility

The incompatibility that occurs when two or more ingredients in a prescription react chemically, altering the properties of the medication.

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Physical Incompatibility

The incompatibility that occurs when two or more ingredients in a prescription physically interact, affecting the appearance or stability of the medication.

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Dry Granulation

A tablet manufacturing method that uses a dry powder mixture, compresses it into a slug, grinds the slug into granules, and then compresses the granules into tablets.

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Direct Compression

A tablet manufacturing method where the powder mixture is directly compressed into tablets without any intermediate granulation step.

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Lubricant

A substance added to the tablet powder mixture to make it flow more easily into the tablet press die.

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Drying

The process of removing excess moisture from the granules after they're formed.

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Competitive plasma protein binding

A situation where two drugs compete for binding to plasma proteins, potentially leading to increased free concentration of one drug and its side effects.

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Enzyme induction

Drugs that induce liver enzymes increase the metabolism of other drugs, lowering their concentration in the blood.

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Enzyme inhibition

Drugs that inhibit liver enzymes decrease the metabolism of other drugs, increasing their concentration in the blood.

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Drug elimination based on urine pH

Acidic drugs are more easily eliminated in alkaline urine, and basic drugs are more easily eliminated in acidic urine.

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Competitive renal elimination

Drugs that compete for active transport mechanisms in the kidneys can lead to accumulation of the drug with lower affinity, potentially increasing its toxicity.

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Increased GI motility and drug absorption

Drugs that increase gastrointestinal motility can reduce the absorption of other drugs.

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Decreased GI motility and drug absorption

Drugs that decrease gastrointestinal motility can enhance the absorption of other drugs.

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Drugs affecting GI motility

Some drugs, such as acetyl choline and metoclopramide, increase gastric motility, leading to reduced drug absorption.

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Synergistic Action

When two drugs are combined and one enhances the other's effect, leading to a greater therapeutic effect or increased toxicity.

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Adverse Action on Same Organ

When two drugs have adverse effects on the same organ, such as the ear, leading to an increased risk of damage.

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Antagonistic Action

When two drugs have opposite effects, leading to a reduced effectiveness of one or both drugs.

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Pharmacokinetic Interactions

A drug interaction where one drug alters the absorption, distribution, metabolism, or excretion of another drug, leading to changes in its plasma concentration and potentially its therapeutic effect or toxicity.

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Pharmacodynamic Interactions

A drug interaction where one drug alters the activity of another drug at the target site or receptor level, leading to an increase or decrease in its effect.

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Drug Concentration Increase

A drug interaction where one drug increases the plasma concentration of another drug, potentially leading to increased therapeutic effect or toxicity.

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Drug Concentration Decrease

A drug interaction where one drug decreases the plasma concentration of another drug, potentially leading to reduced therapeutic effect.

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Oxidation

A chemical reaction where oxygen is added to a substance, resulting in a change in its chemical composition. This can lead to the formation of new compounds, often with different physical and chemical properties.

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Hydrolysis

A chemical reaction that involves the breaking of a chemical bond by the addition of water. This can decompose a compound into smaller molecules.

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Polymerization

A chemical reaction where small molecules combine to form long chains, resulting in a large molecule called a polymer. This can alter the properties of a substance, potentially leading to undesired effects.

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Isomerization

A chemical reaction where the arrangement of atoms within a molecule changes, producing a compound with the same chemical formula but different properties. This can impact a drug's activity and stability.

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Optical Isomerization

A type of isomerization involving the change in spatial arrangement of a chiral molecule. This can affect a drug's biological activity and effectiveness.

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Replacing O2 with N2

A strategy used to prevent oxidation of a drug by replacing oxygen with nitrogen gas. This is especially useful for drugs sensitive to oxidation.

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Selecting appropriate solvent

A method to prevent hydrolysis by selecting a suitable solvent that does not facilitate the breakdown of the drug. This is particularly important for drugs susceptible to chemical reaction with water.

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Adding hygroscopic agents

A method to prevent hydrolysis by adding substances that bind water and reduce its availability. This helps protect the drug from chemical breakdown caused by water.

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Glidants

A type of lubricant that specifically reduces friction between powder particles, aiding in smooth flow during tablet production.

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Coloring Agents

Substances added to tablets to enhance their visual appeal or distinguish different formulations.

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Sweeting Agents

Substances added to tablets to mask unpleasant tastes, making medication more palatable.

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Flavoring Agents

Substances added to tablets to enhance their flavor or aroma, making them more appealing to patients.

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Wet Granulation Method

The process of mixing powdered ingredients and adding a liquid binder to form a wet mass, which is then dried and compressed into tablets.

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Diluent - What are they?

A substance used in tablet formulations to increase the bulk of the tablet and make it easier to compress. Examples include lactose, starch, and mannitol.

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Drying Granules

The process of removing excess moisture from tablet granules, ensuring they are dry enough for compression. It can occur with various methods such as tray drying or fluid-bed drying.

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Wet Granulation - How is it done?

This method involves blending the main active ingredient, diluent, and disintegrant together. Then, a binding agent solution is added with stirring. The mixture is passed through a sieve, dried, and compressed into tablets.

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Picking

A small surface of the tablet is removed during compression, resulting in a pitted surface instead of a smooth one.

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Sticking

The tablet sticks to the die wall during compression, preventing the lower punch from ejecting the tablet.

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Capping

A tablet separates partially or completely from the top or bottom crowns.

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Lamination

The tablet breaks into two or more distinct layers.

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Mottling

Unequal distribution of color on the tablet surface.

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Hardiness Variation

The tablet does not break down in the required time.

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Binding in the Die

The ejection of tablets is difficult, resulting in rough edges.

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Weight Variation

Uneven weight of tablets due to factors like poor flow of granules, size variation, and poor mixing.

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Study Notes

Oxidizing Agents

  • Oxidizing agents (e.g., chlorate, dichromate, permanganate, nitrate, sodium peroxide, silver nitrate, silver oxide) react violently when ground in a mortar with a reducing agent (e.g., sulfides, sulfur, tannic acid, charcoal).
  • Solution:
    • Comminute each salt separately.
    • Subject to minimum pressure.

Special Powders

Effervescent Powders

  • Definition: A mixture of organic acid and alkali that effervesces when exposed to water due to the reaction between the acid and base, releasing carbon dioxide.
  • Examples: Citric or tartaric acids with sodium carbonate or bicarbonate.
  • Advantages of the liberated carbon dioxide:
    • Masks bitter and nauseous taste.
    • Promotes gastric secretions, accelerating absorption.
    • Acts as a carminative.
    • Has a psychologically positive effect, particularly on children.
  • Formulation:
    • Bulk powders or divided powders:
      • Packed in separate packages of contrasting colors.
      • Mixed with water at the time of dosing.
      • Liquid is consumed after the reaction subsides.
    • Effervescent Granules:
      • Sweetened effervescent powders formulated in granules.

Methods of Granulation

Wet Granulation

  • Procedure:
    • Mix powders without pressure in a suitable container.
    • Add alcohol in portions, stirring until a dough-like mass forms.
    • Pass the materials through sieve #6.
    • Dry the resulting granules at a temperature not exceeding 50°C.
    • Pack granules in airtight containers.

Dry Granulation

  • Procedure:
    • Dry all ingredients (except citric acid monohydrate) and pass through sieve #60.
    • Thoroughly mix powders and add citric acid crystals (un-effloresced).
    • Spread the mixture in a shallow dish and place it in a preheated oven (99-105°C).
    • Allow crystallization of citric acid to take place.
    • Stir the powders in a water bath to prevent overheating.
    • Stir until the powders become moist and form a doughy mass.
    • Granulate by passing through sieve #6 and dry.

Packaging

  • Effervescent granules or powders have a short shelf life, especially in wide-mouthed, screw-capped containers.
  • Stability of granules and powders is improved by packaging in tightly sealed aluminum bags.

Test Evaluation of Effervescent Powders

  • Weigh 0.25g of powder, add 5ml distilled water, calculate:
    • Effervescence time.
    • Carbon dioxide volume produced.
    • Duration period for complete effervescence.
    • Solution purity after effervescence.

Capsules

  • Definition: Solid unit dosage forms that encapsulate one or more medicinal ingredients in a small shell or container, usually made of gelatin.
  • Advantages:
    • Mask taste and odor of unpleasant drugs.
    • Easy to swallow due to slipperiness when moist.
    • Fewer adjuncts are required compared to tablets.
    • Easily and quickly digested in the gastrointestinal tract.
    • Economical.
    • Easy to handle and carry.
    • Shells can be opacified or colored for protection.
  • Disadvantages:
    • Hygroscopic drugs can absorb water from the shell, making it brittle.
    • Concentrated solutions may cause stomach irritation if not diluted beforehand.

Types of Capsules

  • Hard gelatin capsules: Enclose solid drug ingredients.
  • Soft gelatin capsules: Enclose liquid and semisolid drug ingredients.
  • Enteric coated capsules: Designed to dissolve in the intestine, not the stomach
  • Sustained release capsules: Release drug ingredients slowly over a period of hours.

Difficulties in Filling Capsules

  • Adding hygroscopic powders to capsules can absorb water, causing cracking.
  • Magnesium bicarbonate or MgO can be added to address this issue.
  • Use diluents (e.g., sucrose) to increase the bulk of smaller drug quantities for easier filling.
  • Place incompatible ingredients in smaller capsules and then those in larger capsules.

Soft Gelatin Capsules

  • Soft, flexible, single-piece shells made from gelatin and plasticizers.
  • Can't be opened, only ruptured.
  • Fill with liquid or semisolids.

Ophthalmic Ointments

  • Can be packaged in unit dose capsules.

Enteric Coated Capsules

  • Capsule designed to dissolve in the intestine, delaying drug release until it reaches that point.

Sustained Release Capsules (Spansules)

  • Powdered drug converted into pellets that are coated (increasing thickness in stages) to release the drug over time periods.

Quality Control of Capsules

  • Quality control tests are varied, depending on the manufacturing scale and method.

Packaging and Storage of Capsules

  • Store in closed containers in a cool environment.
  • Pharmaceutical Aspects:
    • Drug availability from solution > suspension > powder-filled capsule > compressed tablet > coated tablet.
    • Liquid drug form, suspensions can improve the bioavailability of drugs,
    • Orally administered drugs, particularly chronic ones, can affect gastric tolerance.

Tablets

  • Definition: Solid dosage form produced by dry or wet granulation or direct compression containing medicaments with or without excipients to elicit a desired pharmacological response.

  • Advantages:

    • Compact and easily portable.
    • Easy to swallow.
    • Ease of compliance for patients.
    • Bitter taste can be masked by coating.
    • Cheaper than other solid medications.
  • No need for measuring the exact dose.

  • Disadvantages of Tablets:

    • Difficulty in swallowing for children and older adults.
    • Slow dissolution profile
  • How to Achieve Good Tablets:

    • Accurate and uniform weight.

    • Proper distribution of drug within the tablets.

    • Appropriate sizes and shapes, aiding in administration.

    • Stability against disintegration in the stomach

    • Physical and chemical stability for storage.

    • Avoid breakage in transit, physical appearance.

  • Manufacturing Defects to Avoid

    • manufacturing defects need to be avoided.
  • Types of Tablets

Molded tablets

  • Created from moist, rapidly dissolving material pressed into a mold.

Compressed tablets

  • Powders compressed into a specific size or shape.

Chewable tablets

  • Generally for children or patients who have difficulty swallowing.

  • Disintegrates quickly, acceptable taste, and flavor

Soluble tablets

  • Dissolves fully in liquids

Sugar-coated tablets

  • Used to mask unpleasant taste

Film-Coated Tablets

  • Improved stability from atmospheric conditions

Enteric-coated tablets

  • Release of drug in the intestine

Multi-layered tablets

  • Contains different active ingredients

Delayed-release tablets

  • Prolonged release of medication

Press-coated tablets

  • Created from other compressed tablets.

  • Used to combine incompatible ingredients

Buccal tablets and Sublingual tablets

  • Designed to dissolve in the oral cavity

Lozenges

  • Dissolved slowly in the mouth, providing continuous action.

Effervescent tablets

  • Drug containing sodium bicarbonate and citric acid or tartaric acid, effervescing when exposed to water

Vaginal tablets

  • Special shape for ease of insertion.

Implantation tablets

  • Insertion under the skin

Tablet Preparation Methods

  • Wet granulation method
  • Dry granulation method
  • Direct compression method

Tablet Evaluation Tests

  • General Appearance
  • Tablet Thickness
  • Weight Variation Test
  • Hardness test
  • Friability Test
  • Disintegration test
  • Dissolution test
  • Uniformity of Content

Packaging and Storage of Tablets

  • Store in well-closed containers in a cool, dry place to maintain quality and stability.

Drug Incompatibilities

  • Definition: When two or more ingredients are combined, the resulting product has undesired physical, chemical or therapeutic changes which can negatively impact safety of the drug.

  • Classification:

    • Therapeutic incompatibilities
    • Chemical incompatibilities
    • Physical incompatibilities
  • Causes of incompatibility:

    • Drug interactions
    • Overdose
    • Improper dosage
    • Incorrect dosage form

Alterations in Drug Elimination from the Kidney

  • Some drugs depend on pH to be eliminated from the kidney, affected by other drugs that change the pH

  • Some drugs are eliminated via active transport.

Drug Interactions in General

  • Inhibitory or promotional effects on the activity of a drug.

  • Drugs that affect absorption, distribution, metabolism, or excretion rates of other drugs.

Additional Notes

  • Various types of tablet preparation or capsule preparation processes exist.

  • Methods are selected based on the specific needs or characteristics of the drug.

  • Proper storage and handling of capsules and tablets are crucial to maintain quality and efficacy.

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Description

Test your knowledge about the formulation and preparation of pharmaceutical tablets. This quiz covers key aspects such as binding agents, lubrication, disintegration, and tablet characteristics essential for pharmaceutical applications. Perfect for students studying pharmacy or related fields.

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