Drug Conjugates Technology Drives Continuous Upgrades in Precision Medicine
Release time:
2026-01-19
1. Key Technological Pathways under the Concept of Precision Medicine
Against the backdrop of the deepening concept of precision medicine, Drug Conjugates are gradually becoming an important direction in innovative drug development. These molecules combine highly effective drugs with targeted carriers to achieve targeted action on diseased tissues, thereby improving efficacy and reducing systemic side effects.

2. Core Components of Drug Conjugates
Typical Drug Conjugates usually consist of three parts: a targeting molecule, a linker, and a drug payload. The targeting molecule is responsible for identifying specific cells or tissues, the linker controls the timing and method of drug release, and the drug payload directly exerts the therapeutic effect and the targeting molecule is often comprised of a small molecule, peptide, oligonucleotide, antibody, radionuclide, virus like particles, or cells. The design balance between these three components determines the safety and effectiveness of the product.
3. Technological Challenges and Research Priorities
In the development of Drug Conjugates, chemical stability of the linker, uniformity of the payload, and in vivo release mechanisms are key challenges in research and development. With the continuous optimization of linker technology and coupling strategies, more and more drug conjugate projects are entering clinical research stages, driving the continuous advancement of precision medicine.
As technology platforms gradually mature, Drug Conjugates are expected to achieve broader applications in oncology, autoimmune diseases, and other complex diseases, becoming an important component of the precision medicine system.
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1. Key Technological Pathways under the Concept of Precision Medicine
Against the backdrop of the deepening concept of precision medicine, Drug Conjugates are gradually becoming an important direction in innovative drug development. These molecules combine highly effective drugs with targeted carriers to achieve targeted action on diseased tissues, thereby improving efficacy and reducing systemic side effects.

2. Core Components of Drug Conjugates
Typical Drug Conjugates usually consist of three parts: a targeting molecule, a linker, and a drug payload. The targeting molecule is responsible for identifying specific cells or tissues, the linker controls the timing and method of drug release, and the drug payload directly exerts the therapeutic effect and the targeting molecule is often comprised of a small molecule, peptide, oligonucleotide, antibody, radionuclide, virus like particles, or cells. The design balance between these three components determines the safety and effectiveness of the product.
3. Technological Challenges and Research Priorities
In the development of Drug Conjugates, chemical stability of the linker, uniformity of the payload, and in vivo release mechanisms are key challenges in research and development. With the continuous optimization of linker technology and coupling strategies, more and more drug conjugate projects are entering clinical research stages, driving the continuous advancement of precision medicine.
As technology platforms gradually mature, Drug Conjugates are expected to achieve broader applications in oncology, autoimmune diseases, and other complex diseases, becoming an important component of the precision medicine system.
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1. Key Technological Pathways under the Concept of Precision Medicine
Against the backdrop of the deepening concept of precision medicine, Drug Conjugates are gradually becoming an important direction in innovative drug development. These molecules combine highly effective drugs with targeted carriers to achieve targeted action on diseased tissues, thereby improving efficacy and reducing systemic side effects.

2. Core Components of Drug Conjugates
Typical Drug Conjugates usually consist of three parts: a targeting molecule, a linker, and a drug payload. The targeting molecule is responsible for identifying specific cells or tissues, the linker controls the timing and method of drug release, and the drug payload directly exerts the therapeutic effect and the targeting molecule is often comprised of a small molecule, peptide, oligonucleotide, antibody, radionuclide, virus like particles, or cells. The design balance between these three components determines the safety and effectiveness of the product.
3. Technological Challenges and Research Priorities
In the development of Drug Conjugates, chemical stability of the linker, uniformity of the payload, and in vivo release mechanisms are key challenges in research and development. With the continuous optimization of linker technology and coupling strategies, more and more drug conjugate projects are entering clinical research stages, driving the continuous advancement of precision medicine.
As technology platforms gradually mature, Drug Conjugates are expected to achieve broader applications in oncology, autoimmune diseases, and other complex diseases, becoming an important component of the precision medicine system.
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1. Key Technological Pathways under the Concept of Precision Medicine
Against the backdrop of the deepening concept of precision medicine, Drug Conjugates are gradually becoming an important direction in innovative drug development. These molecules combine highly effective drugs with targeted carriers to achieve targeted action on diseased tissues, thereby improving efficacy and reducing systemic side effects.

2. Core Components of Drug Conjugates
Typical Drug Conjugates usually consist of three parts: a targeting molecule, a linker, and a drug payload. The targeting molecule is responsible for identifying specific cells or tissues, the linker controls the timing and method of drug release, and the drug payload directly exerts the therapeutic effect and the targeting molecule is often comprised of a small molecule, peptide, oligonucleotide, antibody, radionuclide, virus like particles, or cells. The design balance between these three components determines the safety and effectiveness of the product.
3. Technological Challenges and Research Priorities
In the development of Drug Conjugates, chemical stability of the linker, uniformity of the payload, and in vivo release mechanisms are key challenges in research and development. With the continuous optimization of linker technology and coupling strategies, more and more drug conjugate projects are entering clinical research stages, driving the continuous advancement of precision medicine.
As technology platforms gradually mature, Drug Conjugates are expected to achieve broader applications in oncology, autoimmune diseases, and other complex diseases, becoming an important component of the precision medicine system.
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