DOI: https://doi.org/10.63345/ijrmp.org.v9.i9.1
Lavanya Reddy
Independent Researcher
Sambalpur, Odisha, India
Abstract
Recent advancements in additive manufacturing have propelled 3D printing technology into the pharmaceutical arena. This manuscript explores the impact of 3D-printed drugs on personalized medicine and dosage precision. The integration of 3D printing in drug production facilitates the design of individualized dosage forms and drug release profiles, addressing the patient-specific needs that conventional manufacturing methods often overlook. In our investigation, we review the evolution of 3D printing applications in the pharmaceutical industry, discuss how these innovations contribute to tailoring therapy based on genetics, disease state, and metabolic factors, and highlight the enhanced dosage precision achievable with this technology. Our literature review—focusing on studies published up to 2019—demonstrates both the technological promise and the regulatory, manufacturing, and quality-control challenges that persist. A methodological framework based on experimental formulation and in vitro testing is proposed to compare the efficacy, stability, and release kinetics of 3D-printed dosage forms versus traditionally manufactured tablets. Our preliminary results indicate that 3D printing not only allows for fine-tuning of drug dosages but also provides a platform for complex drug geometries that can modify pharmacokinetics in a controlled manner. Overall, the integration of 3D printing in pharmaceutical manufacturing promises to revolutionize personalized medicine by ensuring that patients receive medications tailored exactly to their therapeutic needs, potentially reducing adverse effects and improving compliance. The paper concludes with recommendations for future research to address scalability, regulatory challenges, and integration into clinical practice.
Keywords
3D printing, personalized medicine, dosage precision, additive manufacturing, pharmaceutical technology
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