{"title":"From Unwanted Annoyances to Oral Delivery Saviors: The Rollercoaster Journey of Amorphous Drugs.","authors":"Lynne S Taylor, George Zografi","doi":"10.1021/acs.molpharmaceut.5c00013","DOIUrl":null,"url":null,"abstract":"<p><p>The benefits and disadvantages of amorphous drugs have been topics of discussion for nearly a century. In the post-World War II era when drug discovery burgeoned, amorphous drugs were largely regarded as unfavorable forms for commercial products. This sentiment began to change as the number of poorly water-soluble drugs, which targeted a broader range of disease states and emerged from high throughput screening assays, began to increase. The solubility advantage of amorphous drugs was long recognized at this juncture, but unease persisted over potential conversions back to the less soluble crystal form during product storage. Successful development of early amorphous products based on amorphous solid dispersion formulations, where a suitable polymer is molecularly mixed with the drug resulting in inhibition of drug crystallization, gradually mitigated concerns. This historical perspective of amorphous drugs provides an overview of timelines and key milestones and culminates by considering remaining challenges and the future outlook.</p>","PeriodicalId":52,"journal":{"name":"Molecular Pharmaceutics","volume":" ","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acs.molpharmaceut.5c00013","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
The benefits and disadvantages of amorphous drugs have been topics of discussion for nearly a century. In the post-World War II era when drug discovery burgeoned, amorphous drugs were largely regarded as unfavorable forms for commercial products. This sentiment began to change as the number of poorly water-soluble drugs, which targeted a broader range of disease states and emerged from high throughput screening assays, began to increase. The solubility advantage of amorphous drugs was long recognized at this juncture, but unease persisted over potential conversions back to the less soluble crystal form during product storage. Successful development of early amorphous products based on amorphous solid dispersion formulations, where a suitable polymer is molecularly mixed with the drug resulting in inhibition of drug crystallization, gradually mitigated concerns. This historical perspective of amorphous drugs provides an overview of timelines and key milestones and culminates by considering remaining challenges and the future outlook.
期刊介绍:
Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development.
Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.