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Related Concept Videos

Design Example: Resistive Touchscreen01:14

Design Example: Resistive Touchscreen

A device engineer plays a crucial role in designing user interfaces for mobile devices. One such interface is the resistive touchscreen, which fundamentally consists of two metallic layers: a flexible upper layer and a rigid lower layer, separated by a narrow gap. The high resistance between these two layers is a key characteristic of this design.
When a user touches the screen, the two layers make contact at a specific point known as the touchpoint. This contact reduces the resistance between...
Design Example01:23

Design Example

The innovation of touch-tone telephony revolutionized the telecommunications industry by replacing the traditional rotary dial with a dual-tone multi-frequency (DTMF) signaling system. This system uses a matrix-style keypad with buttons arranged in four rows and three columns, creating 12 distinct signals each assigned to a pair of frequencies. Each button press results in a simultaneous generation of two sinusoidal tones – one from a low-frequency group (697 to 941 Hz) and one from a...
Design Consideration01:22

Design Consideration

Designing a structure involves a series of considerations, primarily the material's ultimate strength, calculated through tests that measure changes under increased force until the material reaches its breaking point or limit. The ultimate load, where the material breaks, is divided by its original cross-sectional area, resulting in the ultimate normal stress or strength. The ultimate shearing stress is another significant factor taken into account.
The factor of safety is another key aspect...
Biopharmaceutical Factors Influencing Drug Product Design: Overview01:22

Biopharmaceutical Factors Influencing Drug Product Design: Overview

Rational drug product design integrates knowledge of the drug’s physicochemical properties, formulation components, manufacturing techniques, and intended route of administration. Each factor influences the drug’s performance, including how it is released, absorbed, and eliminated in the body.The physicochemical properties of a drug—such as solubility, stability, and particle size—affect its compatibility with excipients and the choice of dosage form. Excipients, though pharmacologically...
Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules01:18

Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules

Bioequivalence in generic drugs, such as tablets and capsules, refers to their pharmaceutical equivalence to the brand-name counterparts. However, for therapeutic equivalence, manufacturers must also consider physical attributes like size, shape, and weight (FDA Guidance for Industry, December 2003). Discrepancies in these aspects could impact patient compliance and cause medication errors. For instance, swallowing difficulties, often experienced with larger tablets or capsules, can lead to...

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Current State of Minitablet Product Design: A Review.

Saikishore Meruva1, Aditya B Singaraju1, Bhavani Prasad Vinjamuri2

  • 1University of Iowa, College of Pharmacy, Iowa City, IA 52242, USA.

Journal of Pharmaceutical Sciences
|February 18, 2024
PubMed
Summary

Minitablets (MTs) are increasingly popular for personalized medicine and flexible dosing. Research shows MTs are highly acceptable for infants and elderly patients, overcoming swallowing difficulties.

Keywords:
Minitablets, Oral solid dosage forms, Pediatric, Geriatric, Minitablet applications, Tablet compresssion, Coating, Regulatory, Adherence, Acceptability

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Area of Science:

  • Pharmaceutical technology
  • Drug delivery systems
  • Patient-centric formulations

Background:

  • Minitablets (MTs) have seen a surge in research interest over the past two decades.
  • Advances in manufacturing and characterization have resolved earlier development challenges.
  • MTs offer advantages for personalized medicine, dose titration, and taste masking.

Purpose of the Study:

  • To review the current applications and advancements in minitablet technology.
  • To assess the acceptability and adherence of MTs in pediatric and geriatric populations.
  • To discuss manufacturing, characterization, packaging, and regulatory aspects of MTs.

Main Methods:

  • Literature review of publications in Scopus and PubMed.
  • Analysis of research on MT swallowability, acceptability, and palatability.
  • Examination of manufacturing processes, characterization techniques, and dispensing methods.

Main Results:

  • Minitablets are a viable and highly acceptable dosage form for pediatric and geriatric patients.
  • MTs address challenges in swallowing, taste, and flexible dosing.
  • Significant progress has been made in MT tooling, manufacturing, and characterization.

Conclusions:

  • Minitablets represent a significant advancement in drug delivery, particularly for specific patient populations.
  • The acceptability and manufacturing of MTs have improved, supporting their wider adoption.
  • Further research and regulatory considerations are key to maximizing MT potential.