Introduction
Tablets are solid dosage forms containing one or more active pharmaceutical ingredients (APIs) along with suitable excipients, which are compacted or molded into various shapes and sizes. They are among the most common and convenient forms of medication delivery due to their simplicity, ease of administration, accurate dosage, portability, and stability. Tablets are designed to release their active ingredients at a specific rate, in a specific location, or over a specified period, depending on the desired therapeutic effect.
Tablets can be manufactured through various processes, including direct compression, wet granulation, and dry granulation. Each method involves a unique set of steps and requirements to ensure the production of high-quality tablets that meet stringent standards of efficacy, safety, and patient compliance. The choice of manufacturing method depends on the properties of the active ingredients and excipients, the desired tablet characteristics, and the intended use of the tablet.
Ideal Characteristics of Tablets
An ideal tablet should possess the following characteristics:
1. Uniformity:
– Content Uniformity: Each tablet should contain the exact amount of active ingredient as stated on the label to ensure consistent therapeutic effect.
– Weight Uniformity: The weight of each tablet should be consistent within a narrow range, complying with pharmacopeial standards to ensure dose accuracy.
2. Mechanical Strength:
– Hardness: Tablets should have sufficient hardness to withstand mechanical stresses during packaging, transportation, and handling without breaking or chipping.
– Friability: Tablets should not be too friable (prone to crumbling) but also not too hard, which can affect the dissolution rate and, consequently, the bioavailability of the drug.
3. Disintegration:
– Disintegration Time: Tablets should disintegrate into smaller particles or granules within a specified time frame in the gastrointestinal tract to facilitate the release of the active ingredient.
4. Dissolution:
– Dissolution Rate: The active ingredient must dissolve in gastrointestinal fluids at a rate sufficient to ensure its availability for absorption into the bloodstream. The dissolution rate is critical for the onset, intensity, and duration of the therapeutic effect.
5. Stability:
– Physical Stability: Tablets should maintain their shape, size, and appearance under various environmental conditions such as temperature, humidity, and light.
– Chemical Stability: The active ingredient and excipients should remain chemically stable, without degradation or interaction, throughout the shelf life of the tablet.
– Microbiological Stability: Tablets should be free from microbial contamination and remain microbiologically stable.
6. Palatability:
– Taste and Odor: Especially important for chewable or orally disintegrating tablets, palatability ensures patient compliance. Tablets should not have an unpleasant taste or odor.
7. Appearance:
– Aesthetic Quality: Tablets should have an elegant appearance with uniform size, shape, and color, free from any physical defects such as chips or cracks. This enhances acceptability and confidence in the product.
8. Non-Toxic and Non-Irritant:
– Safety: All components of the tablet, including active ingredients and excipients, should be non-toxic, non-irritating, and safe for use within the intended dose range.
Classification of Tablets
Tablets can be classified based on several criteria, including the route of administration, method of manufacture, and intended purpose:
1. Based on Route of Administration:
– Oral Tablets: Designed to be swallowed and absorbed from the gastrointestinal tract.
– Conventional Tablets: Immediate-release formulations designed to disintegrate and release their medication quickly, e.g., aspirin tablets.
– Chewable Tablets: Intended to be chewed before swallowing, often for rapid onset of action or ease of use, e.g., antacid tablets.
– Effervescent Tablets: Dissolve in water before administration, releasing carbon dioxide to form a solution, e.g., vitamin C tablets.
    – Sublingual Tablets,: Placed under the tongue for rapid absorption through the mucous membranes, bypassing the first-pass metabolism, e.g., nitroglycerin tablets.
– Buccal Tablets: Placed in the buccal cavity (between the cheek and gums) for absorption through the oral mucosa, providing a sustained release, e.g., fentanyl buccal tablets.
– Vaginal Tablets: Designed to be inserted into the vagina to provide a local therapeutic effect, e.g., clotrimazole tablets for treating vaginal infections.
– Rectal Tablets: Intended for insertion into the rectum for either local or systemic effects, e.g., paracetamol suppositories for fever and pain.
– Implant Tablets: Surgically implanted in the body to provide a prolonged release of medication, e.g., contraceptive implants.
2. Based on Method of Manufacture:
– Compressed Tablets: Manufactured by compressing powdered ingredients into a solid dosage form using a tablet press.
– Single Compressed Tablets: Consist of a single layer of powder or granules, e.g., most common over-the-counter tablets.
– Multi Compressed Tablets: Consist of multiple layers or a core and shell design to separate incompatible ingredients or to control the release of medication, e.g., biphasic or triphasic tablets.
– Molded Tablets: Prepared by molding a moist mass of powder into the desired shape and drying it, e.g., tablet triturates, typically used for potent drugs requiring accurate dosing.
3. Based on Purpose:
– Immediate Release Tablets: Formulated to release the active ingredient immediately upon administration, e.g., paracetamol tablets.
– Modified Release Tablets:
– Sustained Release Tablets: Designed to release the active ingredient slowly over an extended period to maintain a consistent drug concentration in the bloodstream, e.g., metformin SR tablets.
– Controlled Release Tablets: Formulated to release the drug at a predetermined rate to maintain constant drug levels over time, e.g., nifedipine CR tablets.
– Delayed Release Tablets: Designed to release the active ingredient at a specific location in the gastrointestinal tract, often to prevent degradation by stomach acid, e.g., enteric-coated aspirin tablets.
– Orally Disintegrating Tablets (ODTs): Disintegrate rapidly in the mouth without the need for water, enhancing convenience for patients with difficulty swallowing, e.g., ondansetron ODT.
– Effervescent Tablets: Contain ingredients that react in water, releasing carbon dioxide to form a fizzy solution, e.g., Alka-Seltzer.
– Chewable Tablets: Designed to be chewed to facilitate faster absorption or for patients who have difficulty swallowing, e.g., calcium tablets.
– Sublingual and Buccal Tablets: Designed for rapid absorption through the mucous membranes of the mouth, bypassing the digestive system, e.g., sublingual nitroglycerin tablets.
– Vaginal and Rectal Tablets: Administered for local or systemic effects, such as hormone replacement or infection treatment, e.g., clotrimazole vaginal tablets.
Conclusion
Tablets are a versatile and widely used dosage form in pharmaceuticals, available in various types to meet specific therapeutic needs and patient preferences. The ideal characteristics of tablets ensure their efficacy, safety, and patient acceptability, making them a cornerstone of modern medication therapy.
