Recent Advances in Drug Delivery and Formulation - Online First
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Gallic Acid: A Potent Antioxidant and Anti-inflammatory Agent in Modern Cosmeceuticals
Authors: Urvashi Saini, Anjali Sharma and Vishnu MittalAvailable online: 26 May 2025More LessThe cosmetics business is a valuable and stable multibillion-dollar business that keeps growing yearly with new, specialized goods. Natural goods contain a wealth of medicinally active chemicals used to treat a wide range of skin problems, including infections, inflammation, and damage caused by UV light and pollution. Cosmeceuticals are a mix of cosmetic and medical chemicals. Based on their main ingredients, they can be used for both beauty and health purposes. Many people think that natural goods are a great way to obtain cosmeceuticals. It has strong anti-inflammatory, antibacterial, anti-cancer, and protective properties. The benefit for the skin has been said to be the most interesting. GA and its products have been used a lot as an adjuvant in many therapeutic formulations, as an alternative to hydro-cortisone in children with atopic dermatitis and other skin diseases, and as an ingredient in cosmetics because they are good for humans. GA is GRAS (generally recognized as safe) by the US Food and Drug Administration. Oxidative stress, which happens when too many free radicals build up, is the main cause of many skin diseases that get worse over time, like aging. Polyphenols, including gallic acid, represent a significant category of naturally occurring antioxidants. They have emerged as potent antioxidants suitable for incorporation into active makeup products. Recent advancements include patent filings related to novel applications and formulations of Gallic acid in cosmetic science that highlight innovative delivery systems, such as nano-formulations enhancing stability and efficacy, as well as its synergistic combinations with other active ingredients to address targeted skin concerns like pigmentation, aging, and sensitivity which meets the demands of modern consumers.
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Recent Expansions and Future Outlook in the Delivery of Poorly Soluble Phytoconstituents through Solid Dispersion Technique
Authors: Bhavesh Sahu, Kalyani Sakure, Ajazuddin1 and Hemant BadwaikAvailable online: 23 May 2025More LessPhytoconstituents, derived from plants, possess significant therapeutic potential but often face challenges such as poor solubility and low bioavailability, limiting their efficacy. Solid dispersion (SD) is a promising approach to improve the solubility and bioavailability of these poorly water-soluble phytoconstituents. By dispersing the active drug in a hydrophilic carrier, solid dispersion enhances the surface area of the drug, improving its dissolution rate and enhancing absorption. This review provides an overview of the various generations of solid dispersions, highlighting the evolution from crystalline carriers in first-generation solid dispersions to the more advanced amorphous solid solutions in second and third-generation formulations, which offer enhanced solubility and bioavailability. The article also discusses various techniques for preparing solid dispersions, including solvent evaporation, melting, and spray-drying methods, and emphasizes the importance of selecting appropriate carriers, such as hydrophilic polymers, to optimize the dissolution rate of phytoconstituents. The study highlighted the recent case studies on several phytochemicals, like alkaloids, glycosides, Polyphenols, etc., demonstrating the effectiveness of solid dispersion in improving their solubility and therapeutic performance. Additionally, the review addresses the challenges related to the solubility of phytoconstituents and their impact on drug absorption, as well as the role of solid dispersion in overcoming these challenges. Overall, solid dispersion technology emerges as a versatile and effective tool for enhancing the oral bioavailability of phytoconstituents, paving the way for more efficient herbal therapies in modern medicine.
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Drug Delivery Strategies for the Management of Attention-deficit/ Hyperactivity Disorder (ADHD): A Case of Differentiated Product Development of Methylphenidate
Authors: Shubham Kamble, Ganesh Deshmukh, Paras Jain, Abhishek Jha and Sanjeevani S. DeshkarAvailable online: 23 May 2025More LessADHD is a common condition that affects many kids in the United States, about 2 to 18 percent of children between 6 and 17 years old. ADHD manifests as hyperactivity, impulsivity, and inattention, impacting various aspects of life. Effective management involves a combination of psychostimulant medication, such as methylphenidate, and behavioral therapy. Modified-release formulations, including chewable tablets, transdermal patches, and osmotic-controlled release tablets, offer improved treatment adherence and overall quality of life. Understanding the pathophysiology involves neuroimaging studies that reveal alterations in brain regions rich in dopamine receptors. Methylphenidate, a common ADHD medication, works by inhibiting dopamine reuptake, thereby increasing extracellular dopamine levels. Different drug delivery systems, such as extended-release chewable tablets, transdermal patches, and OROS formulations, provide diverse options for individual needs. The advent of innovative formulations like methylphenidate hydrochloride extended-release oral suspension (Quillivant ER) and methylphenidate hydrochloride multilayer extended-release capsules (Aptensio XR) addresses challenges in pediatric medication administration. Recent additions like the orally disintegrating tablet (Cotempla X-ODT) offer convenience and flexibility. Understanding the pharmacokinetics, pharmacodynamics, and benefits of these formulations enhances the ability to tailor ADHD treatment to individual patient needs.
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Advancing Drug Stability Using Non-Aqueous Gels: Properties, Applications, and Emerging Challenges
Authors: Jabin Ahmed, Aians H Kalita, Ghanshyam Das Gupta and Shubham ThakurAvailable online: 21 May 2025More LessThis study explores the emerging potential of non-aqueous gels for topical therapy, examining their unique properties, diverse applications, and the challenges involved in their formulation and clinical use. By highlighting these aspects, the article aims to shed light on the future of localized drug delivery and inspire further research and innovation in this promising field. Additionally, the article addresses the critical need for regulatory considerations, stability testing, and patient acceptability. It also emphasizes the role of non-aqueous gels in revolutionizing dermatological and transdermal therapies, particularly by enhancing the stability of drugs that are hydrolyzed in the presence of water.
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Advancement in Nanotablet Research: An Overview
Available online: 13 May 2025More LessModern technologies such as nanotechnology are being applied in almost every sector to deliver affordable, environmentally friendly products. The integration of nanotechnology in medicine has revolutionized drug delivery systems, with nanotechnology emerging as a promising frontier. This review explores the synthesis and characterization of nanotablet drug formulations designed to enhance their potential across various applications. By employing characterization techniques such as X-ray diffraction, electron microscopy, and physisorption analysis, researchers have developed innovative drug delivery systems like Sophora Alopecuroides nanotablets to treat deadly diseases such as cancer. Evaluation of pre- and post-compression results indicated that nanotablets exhibited good hardness and flow properties, making these formulations potential drug delivery systems for enhanced bioavailability and sustained release properties. Specifically, sublingual sufentanil nanotablets, such as Zalviso®, have demonstrated efficacy in managing moderate to severe pain in healthcare settings when used in conjunction with a PCA device. However, recent regulatory updates indicate changes in the marketing authorization status of Zalviso®. In conclusion, this novel approach for synthesizing nanotablets presents a promising avenue for diverse applications, and based on the results, it is worth considering for future work.
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Identifying Optimized Parameters to Enhance the Productivity of Gas Generating Pellets Using a Dome Type Extruder
Authors: Ronak R. Patel and Dharmik M. MehtaAvailable online: 08 May 2025More LessIntroductionThe extrusion-spheronization process continues to be utilized in pharmaceutical manufacturing, as evidenced by several recent patents and articles. The primary challenge in pelletization via extrusion spheronization is optimizing the production process to achieve high yields of spherical pellets while keeping production costs low. Therefore, this study aimed to identify the ideal parameters for maximizing production rates using a dome extruder while maintaining the desired physical characteristics of the pellets.
MethodsThe pellet formulation comprised apixaban, microcrystalline cellulose, hypromellose, and sodium bicarbonate. The study employed the face-centered central design to assess the impact of various process variables. Key factors included extruder speed, spheronization speed, and spheronization time, which were determined based on the preliminary analyses. Characterization of pellets encompassed measurements of sphericity via aspect ratio, friability, bulk density, and percentage yield.
ResultsThe optimized parameters for extrusion speed spanned from 23 to 27 rpm, while spheronization speed extended from 700 to 900 rpm at 5 min to 7 min of spheronization time, yielding more than 90% of the desired fraction of spherical pellets with good physical properties.
DiscussionIt was discerned that extrusion and spheronization speed emerged as critical process parameters within a defined spheronization time for maximizing production rates while concurrently maintaining satisfactory pellet properties.
ConclusionThis study successfully optimized process parameters for pellet production using a dome-type extruder by employing a Quality by Design (QbD) approach. Key factors influencing pellet yield and quality, such as extrusion speed, spheronization speed, and time, were identified and systematically optimized.
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Advancements and Challenges in Gastroretentive Drug Delivery Systems: A Comprehensive Review of Research Innovation, Technologies, and Clinical Applications
Authors: Ayush Dubey, Mohammad Ovais, Amol Chhatrapati Bisen and A. RajendiranAvailable online: 28 April 2025More LessGastroretentive drug delivery systems (GRDDS) have emerged as a focal point of research and development, attracting substantial attention due to their potential to revolutionize oral drug administration. Their ability to enhance the bioavailability and therapeutic effectiveness of orally administered medications, particularly those with narrow absorption windows or susceptible to gastrointestinal degradation, has spurred considerable interest. By extending gastric residence time, GRDDS offers a pathway to optimize drug absorption while minimizing dosing frequency, thereby improving patient compliance and therapeutic outcomes. This comprehensive review delves into the diverse array of gastroretentive drug delivery approaches, providing in-depth insights into their classification, mechanisms of retention, recent innovations with patented technologies, and existing marketed formulations of the domain. Furthermore, it meticulously examines the challenges inherent in GRDDS implementation and elucidates effective strategies to surmount them. From novel formulation techniques to ingenious drug-carrier systems, this review explores the multifaceted landscape of GRDDS development, shedding light on promising avenues for future research and development. By advancing current knowledge and anticipating future trends, this review serves as a valuable resource for researchers, clinicians, and pharmaceutical professionals navigating the dynamic terrain of gastroretentive drug delivery.
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