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397 Results Found

  • Article
  • Open Access
91 Citations
6,488 Views
21 Pages

Fused deposition modeling (FDM) three-dimensional (3D) printing is being increasingly explored as a direct manufacturing method to product pharmaceutical solid dosage forms. Despite its many advantages as a pharmaceutical formulation tool, it remains...

  • Review
  • Open Access
198 Citations
81,195 Views
23 Pages

25 February 2014

Lubrication plays a key role in successful manufacturing of pharmaceutical solid dosage forms; lubricants are essential ingredients in robust formulations to achieve this. Although many failures in pharmaceutical manufacturing operations are caused b...

  • Review
  • Open Access
93 Citations
36,708 Views
61 Pages

19 August 2013

The objective of this work is to present a review of computational tools and models for pharmaceutical processes, specifically those for the continuous manufacture of solid dosage forms. Relevant mathematical methods and simulation techniques are dis...

  • Review
  • Open Access
43 Citations
7,074 Views
32 Pages

Therapeutic proteins as biopharmaceuticals have emerged as a very important class of drugs for the treatment of many diseases. However, they are less stable compared to conventional pharmaceuticals. Their long-term stability in solid forms, which is...

  • Article
  • Open Access
5 Citations
4,526 Views
12 Pages

Determination of Zn2+ in Solid Pharmaceutical Dosage Forms by Means of Spectrophotometry in Micellar Media: Method Validation

  • Luca Liviu Rus,
  • Anca Maria Juncan,
  • Veronica Isabela Crăciun,
  • Adina Frum,
  • Simona-Codruța Hegheș,
  • Anca Butuca,
  • Carmen Maximiliana Dobrea,
  • Adriana Aurelia Chis,
  • Andrei Catalin Muntean and
  • Claudiu Morgovan
  • + 1 author

28 April 2022

In this study, a spectrophotometric method for the quantitative determination of zinc in a dietary supplement was validated. Zinc forms a ternary complex with Xylenol Orange and cetylpyridinium chloride in acetate buffer at pH = 5.5. The complex exhi...

  • Article
  • Open Access
5 Citations
2,164 Views
9 Pages

R Shiny App for the Automated Deconvolution of NMR Spectra to Quantify the Solid-State Forms of Pharmaceutical Mixtures

  • Piotr Prostko,
  • Jeroen Pikkemaat,
  • Philipp Selter,
  • Michail Lukaschek,
  • Rainer Wechselberger,
  • Tatsiana Khamiakova and
  • Dirk Valkenborg

10 December 2022

Bioavailability and chemical stability are important characteristics of drug products that are strongly affected by the solid-state structure of the active pharmaceutical ingredient (API). In pharmaceutical development and quality control activities,...

  • Article
  • Open Access
10 Citations
3,543 Views
15 Pages

Towards the Development of Novel Diclofenac Multicomponent Pharmaceutical Solids

  • Francisco Javier Acebedo-Martínez,
  • Carolina Alarcón-Payer,
  • Helena María Barrales-Ruiz,
  • Juan Niclós-Gutiérrez,
  • Alicia Domínguez-Martín and
  • Duane Choquesillo-Lazarte

26 July 2022

Multicomponent pharmaceutical materials offer new opportunities to address drug physicochemical issues and to obtain improved drug formulation, especially on oral administration drugs. This work reports three new multicomponent pharmaceutical crystal...

  • Editorial
  • Open Access
2 Citations
981 Views
2 Pages

This Special Issue aims to highlight the interest of characterizing the structural aspects of an API before its formulation, as much work is required between the discovery of a molecule with a therapeutic effect and its formulation [...]

  • Review
  • Open Access
1,510 Views
35 Pages

The Ubiquitous Use of Polyethylene Glycol in Pharmaceutical Design and Development: Technological Aspects and Future Perspectives

  • Iliana Christoforou,
  • Anastasios Kalatzis,
  • Angeliki Siamidi,
  • Marilena Vlachou,
  • Stergios Pispas and
  • Natassa Pippa

24 November 2025

Polyethylene glycol (PEG) has been extensively utilized in drug formulations due to its multifunctional properties, i.e., hydrophilicity and biocompatibility. The roles played by PEG (as a drug delivery carrier and a solubilizer) improve the dissolut...

  • Article
  • Open Access
24 Citations
5,639 Views
18 Pages

Comparative Study of Powder Carriers Physical and Structural Properties

  • Klára Kostelanská,
  • Barbora Blahová Prudilová,
  • Sylva Holešová,
  • Jakub Vlček,
  • David Vetchý and
  • Jan Gajdziok

High specific surface area (SSA), porous structure, and suitable technological characteristics (flow, compressibility) predetermine powder carriers to be used in pharmaceutical technology, especially in the formulation of liquisolid systems (LSS) and...

  • Review
  • Open Access
54 Citations
24,858 Views
38 Pages

22 September 2022

Highly hygroscopic pharmaceutical and nutraceutical solids are prone to significant changes in their physicochemical properties due to chemical degradation and/or solid-state transition, resulting in adverse effects on their therapeutic performances...

  • Review
  • Open Access
59 Citations
8,174 Views
29 Pages

12 August 2022

This review is aimed to provide to an “educated but non-expert” readership and an overview of the scientific, commercial, and ethical importance of investigating the crystalline forms (polymorphs, hydrates, and co-crystals) of active phar...

  • Review
  • Open Access
29 Citations
5,641 Views
33 Pages

Multicomponent solid forms of low molecular weight drugs, such as co-crystals, salts, and co-amorphous systems, are a result of the combination of an active pharmaceutical ingredient (API) with a pharmaceutically acceptable co-former. These solid for...

  • Article
  • Open Access
29 Citations
7,305 Views
18 Pages

Pharmaceutical Cocrystal Development of TAK-020 with Enhanced Oral Absorption

  • Kouya Kimoto,
  • Mitsuo Yamamoto,
  • Masatoshi Karashima,
  • Miyuki Hohokabe,
  • Junpei Takeda,
  • Katsuhiko Yamamoto and
  • Yukihiro Ikeda

18 March 2020

The objective of this study was to improve the solubility of poorly water-soluble drugs by pharmaceutical cocrystal engineering techniques and select the best pharmaceutical forms with high solubility and solubilized formulations for progress from th...

  • Review
  • Open Access
3 Citations
3,313 Views
36 Pages

Advances in Quantitative Analytical Methods for Solid Drugs

  • Yue Tao,
  • Yuhan Gao,
  • Baoxi Zhang,
  • Kun Hu,
  • Yifei Xie,
  • Li Zhang,
  • Shiying Yang and
  • Yang Lu

30 December 2024

The solid form of the drug can directly affect the physicochemical properties, bioavailability, safety, and efficacy of the drug, and its types mainly include amorphous state, single-component polycrystalline, hydrate, solvate, salt, and cocrystal. P...

  • Article
  • Open Access
22 Citations
5,032 Views
21 Pages

Novel Polymorphic Cocrystals of the Non-Steroidal Anti-Inflammatory Drug Niflumic Acid: Expanding the Pharmaceutical Landscape

  • Francisco Javier Acebedo-Martínez,
  • Carolina Alarcón-Payer,
  • Antonio Frontera,
  • Rafael Barbas,
  • Rafel Prohens,
  • Milena Di Crisci,
  • Alicia Domínguez-Martín,
  • Jaime Gómez-Morales and
  • Duane Choquesillo-Lazarte

Any time the pharmaceutical industry develops a new drug, potential polymorphic events must be thoroughly described, because in a crystalline pharmaceutical solid, different arrangements of the same active pharmaceutical ingredient can yield to very...

  • Review
  • Open Access
476 Citations
32,908 Views
33 Pages

Bioavailability Enhancement Techniques for Poorly Aqueous Soluble Drugs and Therapeutics

  • Dixit V. Bhalani,
  • Bhingaradiya Nutan,
  • Avinash Kumar and
  • Arvind K. Singh Chandel

The low water solubility of pharmacoactive molecules limits their pharmacological potential, but the solubility parameter cannot compromise, and so different approaches are employed to enhance their bioavailability. Pharmaceutically active molecules...

  • Article
  • Open Access
14 Citations
7,175 Views
19 Pages

Structure, Solubility and Stability of Orbifloxacin Crystal Forms: Hemihydrate versus Anhydrate

  • Olimpia Maria Martins Santos,
  • Jennifer Tavares Jacon Freitas,
  • Edith Cristina Laignier Cazedey,
  • Magali Benjamim de Araújo and
  • Antonio Carlos Doriguetto

Orbifloxacin (ORBI) is a widely used antimicrobial drug of the fluoroquinolone class. In the official pharmaceutical compendia the existence of polymorphism in this active pharmaceutical ingredient (API) is reported. No crystal structure has been rep...

  • Review
  • Open Access
45 Citations
3,812 Views
21 Pages

Solid multicomponent systems (SMS) are gaining an increasingly important role in the pharmaceutical industry, to improve the physicochemical properties of active pharmaceutical ingredients (APIs). In recent years, various processes have been employed...

  • Review
  • Open Access
74 Citations
10,235 Views
20 Pages

Artificial Neural Networks in Evaluation and Optimization of Modified Release Solid Dosage Forms

  • Svetlana Ibrić,
  • Jelena Djuriš,
  • Jelena Parojčić and
  • Zorica Djurić

18 October 2012

Implementation of the Quality by Design (QbD) approach in pharmaceutical development has compelled researchers in the pharmaceutical industry to employ Design of Experiments (DoE) as a statistical tool, in product development. Among all DoE technique...

  • Review
  • Open Access
114 Citations
12,258 Views
49 Pages

Mechanochemistry: A Green Approach in the Preparation of Pharmaceutical Cocrystals

  • Mizraín Solares-Briones,
  • Guadalupe Coyote-Dotor,
  • José C. Páez-Franco,
  • Miriam R. Zermeño-Ortega,
  • Carmen Myriam de la O Contreras,
  • Daniel Canseco-González,
  • Alcives Avila-Sorrosa,
  • David Morales-Morales and
  • Juan M. Germán-Acacio

Mechanochemistry is considered an alternative attractive greener approach to prepare diverse molecular compounds and has become an important synthetic tool in different fields (e.g., physics, chemistry, and material science) since is considered an ec...

  • Article
  • Open Access
12 Citations
3,365 Views
19 Pages

Enhanced NSAIDs Solubility in Drug–Drug Formulations with Ciprofloxacin

  • Francisco Javier Acebedo-Martínez,
  • Alicia Domínguez-Martín,
  • Carolina Alarcón-Payer,
  • Alejandro Sevillano-Páez,
  • Cristóbal Verdugo-Escamilla,
  • Josefa María González-Pérez,
  • Fernando Martínez-Checa and
  • Duane Choquesillo-Lazarte

7 February 2023

Drug–drug salts are a kind of pharmaceutical multicomponent solid in which the two co-existing components are active pharmaceutical ingredients (APIs) in their ionized forms. This novel approach has attracted great interest in the pharmaceutica...

  • Article
  • Open Access
31 Citations
6,624 Views
22 Pages

Polyvinyl Alcohol-Based 3D Printed Tablets: Novel Insight into the Influence of Polymer Particle Size on Filament Preparation and Drug Release Performance

  • Andrea Gabriela Crișan,
  • Alina Porfire,
  • Rita Ambrus,
  • Gábor Katona,
  • Lucia Maria Rus,
  • Alin Sebastian Porav,
  • Kinga Ilyés and
  • Ioan Tomuță

Three-dimensional printing (3DP) by fused deposition modeling (FDM) has gained momentum as a promising pharmaceutical manufacturing method due to encouraging forward-looking perspectives in personalized medicine preparation. The current challenges th...

  • Article
  • Open Access
38 Citations
12,390 Views
10 Pages

Stability studies represent an essential component of pharmaceutical development, enabling critical evaluation of the therapeutic potential of an active pharmaceutical ingredient (API) or a final pharmaceutical product under the influence of various...

  • Article
  • Open Access
6 Citations
4,120 Views
20 Pages

Submerged Eutectic-Assisted, Solvent-Free Mechanochemical Formation of a Propranolol Salt and Its Other Multicomponent Solids

  • Klaudia Bialek,
  • Zaneta Wojnarowska,
  • Marcin Skotnicki,
  • Brendan Twamley,
  • Marian Paluch and
  • Lidia Tajber

Salt preparation via a solid-state reaction offers a solution to challenges posed by current pharmaceutical research, which include combining development of novel forms of active pharmaceutical ingredients with greener, sustainable synthesis. This wo...

  • Article
  • Open Access
33 Citations
9,412 Views
16 Pages

Solid-State Characterization of Different Crystalline Forms of Sitagliptin

  • Nayana C. F. Stofella,
  • Andressa Veiga,
  • Laiane J. Oliveira,
  • Elisa F. Montin,
  • Itamar F. Andreazza,
  • Marco A. S. Carvalho Filho,
  • Larissa S. Bernardi,
  • Paulo R. Oliveira and
  • Fábio S. Murakami

24 July 2019

Sitagliptin is an inhibitor of the enzyme dipeptidyl peptidase-4, used for the treatment of type 2 diabetes mellitus. The crystal structure of active pharmaceutical solids determines their physical and chemical properties. The polymorphism, solvates...

  • Review
  • Open Access
41 Citations
9,922 Views
30 Pages

31 August 2023

Micro- and nanotechnologies have been intensively studied in recent years as novel platforms for targeting and controlling the delivery of various pharmaceutical substances. Microparticulate drug delivery systems for oral, parenteral, or topical admi...

  • Article
  • Open Access
56 Citations
11,007 Views
11 Pages

Photocurable Bioink for the Inkjet 3D Pharming of Hydrophilic Drugs

  • Giovanny F. Acosta-Vélez,
  • Chase S. Linsley,
  • Madison C. Craig and
  • Benjamin M. Wu

Novel strategies are required to manufacture customized oral solid dosage forms for personalized medicine applications. 3D Pharming, the direct printing of pharmaceutical tablets, is an attractive strategy, since it allows for the rapid production of...

  • Article
  • Open Access
5 Citations
2,664 Views
13 Pages

Complexation: An Interesting Pathway for Combining Two APIs at the Solid State

  • Fucheng Leng,
  • Oleksii Shemchuk,
  • Koen Robeyns and
  • Tom Leyssens

Combining different drugs into a single crystal form is one of the current challenges in crystal engineering, with the number of reported multi-drug solid forms remaining limited. This paper builds upon an efficient approach to combining Active Pharm...

  • Review
  • Open Access
16 Citations
5,914 Views
17 Pages

3D Printing in Solid Dosage Forms and Organ-on-Chip Applications

  • Tarek Kassem,
  • Tanoy Sarkar,
  • Trieu Nguyen,
  • Dipongkor Saha and
  • Fakhrul Ahsan

22 March 2022

3D printing (3DP) can serve not only as an excellent platform for producing solid dosage forms tailored to individualized dosing regimens but can also be used as a tool for creating a suitable 3D model for drug screening, sensing, testing and organ-o...

  • Review
  • Open Access
33 Citations
5,564 Views
32 Pages

Biopolymer Drug Delivery Systems for Oromucosal Application: Recent Trends in Pharmaceutical R&D

  • Natallia V. Dubashynskaya,
  • Valentina A. Petrova and
  • Yury A. Skorik

Oromucosal drug delivery, both local and transmucosal (buccal), is an effective alternative to traditional oral and parenteral dosage forms because it increases drug bioavailability and reduces systemic drug toxicity. The oral mucosa has a good blood...

  • Review
  • Open Access
36 Citations
7,577 Views
18 Pages

Recent Advances in the Application of Characterization Techniques for Studying Physical Stability of Amorphous Pharmaceutical Solids

  • Yanan Wang,
  • Yong Wang,
  • Jin Cheng,
  • Haibiao Chen,
  • Jia Xu,
  • Ziying Liu,
  • Qin Shi and
  • Chen Zhang

23 November 2021

The amorphous form of a drug usually exhibits higher solubility, faster dissolution rate, and improved oral bioavailability in comparison to its crystalline forms. However, the amorphous forms are thermodynamically unstable and tend to transform into...

  • Article
  • Open Access
61 Citations
10,137 Views
14 Pages

Co-Crystal Screening of Diclofenac

  • Christer B. Aakeröy,
  • Angela B. Grommet and
  • John Desper

In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological...

  • Review
  • Open Access
21 Citations
9,981 Views
24 Pages

12 June 2023

One of the major challenges in the development of effective pharmaceutical formulations for oral administration is the poor solubility of active pharmaceutical ingredients. For this reason, the dissolution process and drug release from solid oral dos...

  • Article
  • Open Access
2,935 Views
15 Pages

From Liquid to Solid: Cocrystallization as an Engineering Tool for the Solidification of Pyruvic Acid

  • Camila Caro Garrido,
  • Koen Robeyns,
  • Damien P. Debecker,
  • Patricia Luis and
  • Tom Leyssens

12 May 2023

Pyruvic acid is an organic compound used in various fields (e.g., the pharmaceutical, cosmetic, food, and chemical industries) and subject to constantly growing demand. Pyruvic acid is liquid at room temperature, rendering manipulation less straightf...

  • Article
  • Open Access
556 Views
13 Pages

Crystallization of Four Troglitazone Isomers: Selectivity and Structural Considerations

  • Shinji Matsuura,
  • Koichi Igarashi,
  • Masayuki Azuma and
  • Hiroshi Ooshima

30 September 2025

The control of crystal form in chiral active pharmaceutical ingredients (APIs) is a critical challenge in pharmaceutical development, as differences in solid-state structure can significantly influence physical properties and manufacturing performanc...

  • Article
  • Open Access
13 Citations
4,737 Views
19 Pages

The Quest for Child-Friendly Carrier Materials Used in the 3D Semi-Solid Extrusion Printing of Medicines

  • Eveline E. M. van Kampen,
  • Sejad Ayyoubi,
  • Luc Willemsteijn,
  • Kjeld J. C. van Bommel and
  • Elisabeth J. Ruijgrok

This work gives a brief overview of carrier materials currently used in pharmaceutical studies on the three-dimensional (3D) semi-solid extrusion (SSE) printing of medicines for pediatrics. The suitability of using these carrier materials in pediatri...

  • Review
  • Open Access
46 Citations
19,946 Views
33 Pages

Self-Emulsifying Drug Delivery Systems (SEDDS): Transition from Liquid to Solid—A Comprehensive Review of Formulation, Characterization, Applications, and Future Trends

  • Prateek Uttreja,
  • Indrajeet Karnik,
  • Ahmed Adel Ali Youssef,
  • Nagarjuna Narala,
  • Rasha M. Elkanayati,
  • Srikanth Baisa,
  • Nouf D. Alshammari,
  • Srikanth Banda,
  • Sateesh Kumar Vemula and
  • Michael A. Repka

Self-emulsifying drug delivery systems (SEDDS) represent an innovative approach to improving the solubility and bioavailability of poorly water-soluble drugs, addressing significant challenges associated with oral drug delivery. This review highlight...

  • Review
  • Open Access
68 Citations
13,923 Views
26 Pages

Emerging Artificial Intelligence (AI) Technologies Used in the Development of Solid Dosage Forms

  • Junhuang Jiang,
  • Xiangyu Ma,
  • Defang Ouyang and
  • Robert O. Williams

Artificial Intelligence (AI)-based formulation development is a promising approach for facilitating the drug product development process. AI is a versatile tool that contains multiple algorithms that can be applied in various circumstances. Solid dos...

  • Review
  • Open Access
1 Citations
3,421 Views
16 Pages

Taxus, as a globally prevalent evergreen tree, contains a wealth of bioactive components that play a crucial role in the pharmaceutical field. Taxus extracts, defined as a collection of one or more bioactive compounds extracted from the genus Taxus s...

  • Article
  • Open Access
14 Citations
4,205 Views
19 Pages

Hybrid Manufacturing of Oral Solid Dosage Forms via Overprinting of Injection-Molded Tablet Substrates

  • Han Xu,
  • Farnoosh Ebrahimi,
  • Ke Gong,
  • Zhi Cao,
  • Evert Fuenmayor and
  • Ian Major

Since 3D printing allows for patient-specific dosage forms, it has become a major focus in pharmaceutical research. However, it is difficult to scale up drug product manufacturing. Injection molding has been used in conjunction with hot-melt extrusio...

  • Perspective
  • Open Access
21 Citations
4,467 Views
16 Pages

20 August 2020

At the moment, there are no U.S. Food and Drug Administration (U.S. FDA)-approved drugs for the treatment of COVID-19, although several antiviral drugs are available for repurposing. Many of these drugs suffer from polymorphic transformations with ch...

  • Article
  • Open Access
4 Citations
2,520 Views
15 Pages

17 October 2023

Balsam poplar buds have been used for wound healing and treating irritated skin in traditional medicine. Balsam poplar buds extracts exhibit anti-inflammatory, antioxidant, and antimicrobial effects. In recent years, scientific research has begun to...

  • Article
  • Open Access
2 Citations
3,478 Views
22 Pages

Background: Melt-based 3D printing technologies are currently extensively evaluated for research purposes as well as for industrial applications. Classical approaches often require intermediates, which can pose a risk to stability and add additional...

  • Entry
  • Open Access
53 Citations
9,699 Views
22 Pages

Deep Eutectic Solvents and Pharmaceuticals

  • Sónia N. Pedro,
  • Carmen S. R. Freire,
  • Armando J. D. Silvestre and
  • Mara G. Freire

9 September 2021

Deep eutectic solvents (DES) are eutectic mixtures that present a deviation from the ideal thermodynamic solid–liquid phase behavior, where a significant depression in the melting temperature occurs. If properly designed and chosen, DES may be liquid...

  • Article
  • Open Access
12 Citations
6,296 Views
13 Pages

A continuous-spray granulator (CTS-SGR) is a one-step granulation technology capable of using solutions or suspensions. The present research objectives were, (1) to reduce the manufacturing operations for solid dosage formulations, (2) to make amorph...

  • Article
  • Open Access
18 Citations
7,199 Views
12 Pages

Microcrystalline Cellulose Extracted from Native Plants as an Excipient for Solid Dosage Formulations in Drug Delivery

  • Camila Viera-Herrera,
  • Javier Santamaría-Aguirre,
  • Karla Vizuete,
  • Alexis Debut,
  • Daniel C. Whitehead and
  • Frank Alexis

Excipients represent the complement of the active principle in any pharmaceutical form. Their function is to provide stability, protection, and to ensure absorption of the drug and acceptability in patients. Cellulose is a conventional excipient in m...

  • Article
  • Open Access
18 Citations
5,160 Views
17 Pages

Myth or Truth: The Glass Forming Ability Class III Drugs Will Always Form Single-Phase Homogenous Amorphous Solid Dispersion Formulations

  • Piyush Panini,
  • Massimiliano Rampazzo,
  • Abhishek Singh,
  • Filip Vanhoutte and
  • Guy Van den Mooter

The physical stability of amorphous solid dispersions (ASD) of active pharmaceutical ingredients (APIs) of high glass forming ability (GFA class III) is generally expected to be high among the scientific community. In this study, the ASD of ten-selec...

  • Review
  • Open Access
16 Citations
6,307 Views
14 Pages

A Review of Coformer Utilization in Multicomponent Crystal Formation

  • Nasrul Wathoni,
  • Wuri Ariestika Sari,
  • Khaled M. Elamin,
  • Ahmed Fouad Abdelwahab Mohammed and
  • Ine Suharyani

8 December 2022

Most recently discovered active pharmaceutical molecules and market-approved medicines are poorly soluble in water, resulting in limited drug bioavailability and therapeutic effectiveness. The application of coformers in a multicomponent crystal meth...

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