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Drug Affinity Responsive Target Stability Articles & Analysis

25 news found

A new approach to Amorphous Solid Dispersions with Precellys and Cryolys

A new approach to Amorphous Solid Dispersions with Precellys and Cryolys

Challenges in Pharmaceutical Development Improving the dissolution, solubility, and bioavailability of poorly soluble drugs (BCS Class 2) remains a significant challenge. Amorphous Solid Dispersions (ASDs) are a promising solution, stabilizing drugs in their amorphous form using polymers and low-molecular-weight excipients. However, thermodynamic instability and complex processing steps make ...

ByBertin Technologies


CD Formulation Offers Advanced Transdermal Delivery Enhancement Technologies

CD Formulation Offers Advanced Transdermal Delivery Enhancement Technologies

CD Formulation, a leading force in biotechnology research and development, is at the forefront of revolutionizing transdermal delivery systems. As the demand for non-invasive, efficient drug delivery systems grows, CD Formulation has announced its abilities in providing a few transdermal delivery enhancement technologies. Transdermal Delivery: Overcoming Natural Barriers Traditional transdermal ...

ByCD Formulation


Protheragen-ING Announces Lyophilized Flash-release Formulations Development Capabilities

Protheragen-ING Announces Lyophilized Flash-release Formulations Development Capabilities

Protheragen-ING has recently announced its ability to provide freeze-drying flash-release formulation development services to clients involved in drug discovery and development worldwide. Lyophilized flash-release formulations are advanced drug delivery systems that incorporate the benefits of both lyophilization and flash-release technologies. “Whether customers are trying to develop a ...

ByProtheragen-ING


Huateng Pharma: Empowering ADC Development with Premium Monodispersed PEGs

Huateng Pharma: Empowering ADC Development with Premium Monodispersed PEGs

Changsha, China – Hunan Huateng Pharmaceutical Co., Ltd. is proud to provide high-quality monodispersed polyethylene glycols (PEGs) tailored for the evolving needs of antibody-drug conjugates (ADCs). With the ADC market surpassing $10 billion in 2023 and projected to reach $13.13 billion by 2030, our commitment to innovation and quality is stronger than ever. Among the 15 approved ADCs ...

ByHunan Huateng Pharmaceutical Co. Ltd.


Biopharma PEG Expands GMP Production of Lipids and PEGs to Meet Growing Demand for Lipid Nanoparticles

Biopharma PEG Expands GMP Production of Lipids and PEGs to Meet Growing Demand for Lipid Nanoparticles

Biopharma PEG, a key provider of premium polyethylene glycol (PEG) derivatives, is thrilled to announce a substantial expansion of its large-scale Good Manufacturing Practice (GMP) production capabilities. This strategic move is aimed at addressing the rising global demand for Lipid Nanoparticles (LNPs), which are vital for nucleic acid drug delivery, especially in mRNA-based therapies and ...

ByBiopharma PEG Scientific Inc


Huateng Pharma Introduces Y-Shape PEG NHS

Huateng Pharma Introduces Y-Shape PEG NHS

Huateng Pharma, a global leader in PEG derivatives and a premier CDMO for APIs and intermediates, is excited to announce the launch of its latest product, Y-Shape PEG NHS. This cutting-edge Succinimidyl Carboxymethyl Ester branched 2ARM PEG offers a revolutionary approach to amine PEGylation, enhancing the modification of proteins and other biologics. PEGylation, the technique of attaching a PEG ...

ByHunan Huateng Pharmaceutical Co. Ltd.


CD Formulation Develops, Evaluates, and Utilizes Innovative Drug Delivery Technologies for the Pharmaceutical Industry   

CD Formulation Develops, Evaluates, and Utilizes Innovative Drug Delivery Technologies for the Pharmaceutical Industry  

CD Formulation is making waves in the pharmaceutical industry with its innovative drug delivery technologies. With a focus on sustained and controlled release formulations, as well as liquid, semi-solid, injectable, and nanoformulations, CD Formulation is at the forefront of the industry's efforts to enhance drug efficacy. One of CD Formulation's key technology platforms is its sustained ...

ByCD Formulation


CD Formulation Introduces Microneedle Patch Innovations for Enhanced Drug Delivery Efficiency

CD Formulation Introduces Microneedle Patch Innovations for Enhanced Drug Delivery Efficiency

CD Formulation, a leading innovator in drug delivery technologies, has recently introduced a series of groundbreaking microneedle patch innovations that promise to revolutionize the way drugs are administered. Microneedle patches are a novel drug delivery system that utilizes tiny needles to painlessly penetrate the skin's outer layer and deliver medication directly into the bloodstream. This ...

ByCD Formulation


STEMart Launches New Force Degradation Services to Ensure Drug Stability and Safety

STEMart Launches New Force Degradation Services to Ensure Drug Stability and Safety

STEMart, a US-based provider of comprehensive services for all phases of medical device development, announced the launch of its new Force Degradation Services to help pharmaceutical and medical device companies evaluate the stability of their drug candidates and finished products under a variety of stress conditions, ensuring their safety and efficacy throughout their shelf life. Forced ...

BySTEMart


CD Formulation Excels in Developing and Optimizing Micro-Reservoir Controlled-Release Drug Delivery Systems   

CD Formulation Excels in Developing and Optimizing Micro-Reservoir Controlled-Release Drug Delivery Systems  

CD Formulation has been dedicated to pharmaceutical advancements, showcasing immense expertise in the development and optimization of micro-reservoir controlled-release drug delivery systems. These innovative systems have revolutionized the way medications are administered, enhancing patient comfort and ensuring optimal therapeutic efficacy. Transdermal drug delivery systems are very popular ...

ByCD Formulation


Stability Analysis Plays a Crucial Role in Pharmaceutical Formulation, Highlighted by CD Formulation   

Stability Analysis Plays a Crucial Role in Pharmaceutical Formulation, Highlighted by CD Formulation  

In the field of pharmaceutical formulation, stability analysis is a critical aspect that ensures the safety and efficacy of drugs throughout their shelf life. CD formulation has introduced a series of stability analysis services as a prominent tool for researchers to understand the influence of various factors and tests on the stability of pharmaceutical products. With extensive expertise in ...

ByCD Formulation


CD Formulation Provides Efficient Strategies to Develop and Optimize Microspheres & Microneedles

CD Formulation Provides Efficient Strategies to Develop and Optimize Microspheres & Microneedles

In recent years, the field of drug delivery has experienced significant advancements in the development of innovative delivery systems such as microspheres and microneedles. These advanced systems offer unique benefits, including enhanced drug stability, sustained release, and targeted delivery. However, the successful formulation and optimization of these delivery systems pose significant ...

ByCD Formulation


Pushing the Boundaries of Drug Delivery: CD Formulation's Breakthrough Microsphere and Microneedle Technologies

Pushing the Boundaries of Drug Delivery: CD Formulation's Breakthrough Microsphere and Microneedle Technologies

As medicine continues to advance in this new era, drug delivery methods have been revolutionized to enhance patient comfort, improve treatment outcomes and ensure effective delivery of therapeutic compounds. CD Formulation, a leading pharmaceutical research and development company, has recently unveiled a series of cutting-edge technologies that will further revolutionize and redefine the realm ...

ByCD Formulation


ARAI-2PAM Barda Procurement Award

ARAI-2PAM Barda Procurement Award

Broomfield, Colorado, 10/3/2022. Aktiv Pharma Group (Aktiv) today announced a procurement contract award from the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS). Under this contract (number 75A50122C00082), awarded under the 2004 Project ...

ByAktiv Pharma Group, Inc


FDA Emerging Technology Program

FDA Emerging Technology Program

Broomfield Colorado 6/16/2022. Aktiv Pharma Group (Aktiv) announced today the acceptance of its novel glass-free, film-based flexible primary drug container (PDC) technology for sterile injectables named ARCH, into the US Food and Drug Administration (FDA) Emerging Technology Program (ETP). The ETP is a collaborative effort which supports the FDA’s mission to facilitate modernization in ...

ByAktiv Pharma Group, Inc


Accelerated Shelf-Life Testing to Assess Drug Stability

Accelerated Shelf-Life Testing to Assess Drug Stability

In recent decades, shelf-life prediction is increasingly recognized as an important and necessary part of any new product development. Fully aware of this, CD Formulation, a New York-based CRO company reputed for high-quality drug pre-formulation services, announced earlier this month to have launched long-term accelerated shelf-life testing for drug developers and pharmaceutical companies ...

ByCD Formulation


Aktiv Pharma Group Receives Grant Funding to Develop Tranexamic Acid Autoinjector

Aktiv Pharma Group Receives Grant Funding to Develop Tranexamic Acid Autoinjector

Broomfield Colorado 6/25/2022. Aktiv Pharma Group (Aktiv) announced today a grant award from the U.S. Department of Defense (DOD) Defense Health Agency (DHA) Joint Program Committee 6/Combat Casualty Care Research Program (JPC-6/CCCRP) [1] for the continued development of a tranexamic acid (TXA) autoinjector, targeting proposed indications related to prehospital treatment of severe bleeding. ...

ByAktiv Pharma Group, Inc


CD Formulation Offers Forced Degradation Studies

CD Formulation Offers Forced Degradation Studies

To ensure the safety and efficacy of the drug product, chemical stability is of paramount importance. Earlier this month, CD Formulation announced its decision to launch forced degradation studies to help researchers find ways to promote drug stability. The forced degradation study, also known as stress testing, is carried out to produce representative samples for developing stability-indicating ...

ByCD Formulation


CD Formulation Launches Tailored Solutions for Increased Bioavailability Excipients for Drug Development

CD Formulation Launches Tailored Solutions for Increased Bioavailability Excipients for Drug Development

In a recent statement, the York-based CRO company CD Formulation announces the launch of tailored solutions for increased bioavailability excipients, which aims to tackle the issue of poor bioavailability, a long-lasting challenge in drug development. Many drug candidates unfortunately stopped their way ahead from the discovery pipeline just simply because they are poorly water-soluble, which ...

ByCD Formulation


Pronalyse Unveils Protein Drug Modification Analysis to Move Your Drug Development Program Forward

Pronalyse Unveils Protein Drug Modification Analysis to Move Your Drug Development Program Forward

Pronalyse is a new division of Creative Proteomics, which is an integrated CRO company with rich experience in providing drug development service for over 10 years. The company has recently announced Protein Drug Modification Analysis service to help researchers determine the modification type, modification site, and modification structure of protein drugs. Mature protein medicines have complete ...

ByCreative Proteomics

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