CN
Tides CDMO Services

With four major R&D platforms including peptides, oligonucleotides, high-performance liquid chromatography, and Tides analysis, the Porton Tides CDMO Services Platform is committed to providing integrated CMC solutions for global customers, covering all types of new drugs from pre-clinical to commercial.

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    100+

    Customers

    30+

    Projects (IND/P1/P2/P3/NDA)

    150+

    Scientists

Our Services

    Peptides

    Linear Peptides (<50 aa)

    Cyclic Peptides (<50 aa)

    Peptide Modifications

    Key RSMs and Intermediates

    Oligonucleotides

    ASO, siRNA

    PMO

    Aptamer

    sgRNA

    Oligo Modifications

    Drug Delivery Materials

    Ionizable Lipids/Cationic Lipids

    Polymers for Drug Delivery

    Complex/Conjugate Polysaccharides

    Other Lipids

Peptides

Linear Peptides (<50 aa)

Cyclic Peptides (<50 aa)

Peptide Modifications

Key RSMs and Intermediates

Molecular Type
  • Linear Peptides (<50 aa)
  • Cyclic Peptides (<50 aa)
  • Arginine-rich Peptides
  • Stapled Peptides
  • Peptide Modifications: PEG, lipidation, N-methylation, etc.
  • Key RSMs and Intermediates
  • ADC Drug-Linker and PDC (OEB 5)
Technology
  • Solid/Liquid/Hybrid Strategies Synthetic Solutions
  • Combinate Downstream Technologies with Rp-prep-HPLC, Ionic Exchange, and TFF Technology
  • Pre-formulation Development
  • Comprehensive Analysis and Quality Research
Service Scope
  • mg-g Scale Sample Preparation for Pre-clinical Studies
  • Process Development and Scale-up Mfg. (non-GMP and GMP)
  • Formulation Development and GMP Manufacturing
  • Analytical Method Development, Validation, and Stability Study
  • IND/NDA CMC Dossier
Service Mode
  • Full Time Employee (FTE)
  • Fee for Service (FFS)
Oligonucleotides

ASO, siRNA

PMO

Aptamer

sgRNA

Oligo Modifications

Molecular Type
  • 16~100 mer Oligonucleotides and Derivatives
  • Modified Nucleotides
  • Oligonucleotide Conjugates
  • Custom Monomer
  • Custom Galnac Derivatives
Technology
  • Solid Phase Oligonucleotide Synthesis Technology Platform
  • Ion Exchange, Ultrafiltration, Freeze-drying, and Other Purification and Post-processing Technologies
  • Nucleic Acid Modification and Routine Injection Preparation Research and Development Capability (Including LNP)
  • Comprehensive Analysis and Quality Research
Service Scope
  • mg to g Scale Sample Preparation for Pre-clinical Studies
  • Process Development and Scale-up Manufacturing (non-GMP and GMP)
  • Formulation Development and GMP Manufacturing
  • Analytical Method Development, Validation, and Stability Study
  • IND/NDA CMC Dossier
Service Mode
  • FTE (Full-Time Equivalent)
  • FFS (Fee for Service)
Drug Delivery Materials

Ionizable Lipids/Cationic Lipids

Polymers for Drug Delivery

Complex/Conjugate Polysaccharides

Other Lipids

Molecular Type
  • Polymer-drug Conjugates, Dendrimers, Polypeptides
  • Cationic/Ionizable Lipids, Peg-lipid, Phospholipids
  • GalNAc Derivatives, Modified Monosaccharides, Synthetic Oligo[poly]saccharides
Technology
  • Solid Phase and Liquid Phase Synthesis Technology Platform
  • Combinate Downstream Technologies with prep-HPLC and Rp-prep-HPLC, Ionic Exchange, and TFF Technology
  • Formulations Development and Manufacturing
  • Comprehensive Analysis, Inspection and Quality Research
Service Scope
  • mg-g Scale Sample Preparation for Pre-clinical Studies
  • Process Development and Scale-up Mfg. (non-GMP & GMP)
  • Analytical Method Development, Validation, and Stability Study
  • IND/NDA CMC Dossier
Service Mode
  • FTE (Full-Time Equivalent)
  • FFS (Fee for Service)
  • Case Studies

    More

    Preformulation Strategy- Inception to Completion

    Drug discovery is an exceedingly complex process. Discovering a new chemical entity is in itself a huge accomplishment, which is often possible only after almost two decades of hard experimental work as well as advanced simulation efforts. Therefore, the next stage of the process, determination of toxicity becomes even more crucial as most new chemical entities (NCE) are disqualified if the NCE shows a potential toxic effect, despite any possible therapeutic effect.

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    Facilitating PROTAC Drugs Development with Innovative Processes

    The PROTAC technology, through an innovative mechanism of "degradation rather than inhibition," provides a new pathway for targeting traditionally undruggable proteins and addressing resistance issues.

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    Continuous Improvement of Project Life Cycle Management, Benefiting Customers by Reducing Total Cost

    Continuous Improvement of Project Life Cycle Management, Benefiting Customers by Reducing Total Cost

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    Molecular Modeling and Data Science for De-risking and Cost- saving of Pharmaceutical Development

    Molecular Modeling and Data Science for De-risking and Cost- saving of Pharmaceutical Development

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    Co-processing: Co-Precipitation Technology (CPT) for the Enhancement of Flowability and Bulk Density

    Formulating compressed tablets is one of the most widely used oral solid form dosages. However, a vital first step is choosing a suitable manufacturing approach and the right excipients to support the desired therapeutic effect.

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    ENT-03 GRC Poster

    ENT-03 GRC Poster

    ENT-03 was predicted to be the mammalian equivalent of trodusquemine, based on knowledge of the bile acids produced in mammals, such as 7-HOCA. The individual C-25 isomers of ENT-03 were prepared and both detected in mouse brain. Trodusquemine and ENT-03 have both demonstrated dramatic effects in obesity and insulin resistance. (25S)-ENT-03 was selected for development for the treatment of diabetes and obesity.

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