Peptide Therapeutics

Precision and Control from Lab to Packaged Product

peptides molecule

Peptide development, either through chemical synthesis or as recombinant molecules from cell based platforms present unique scientific and operational challenges. From research and process development to large-scale bioprocessing, scientists and engineers face low yields, productivity, batch variability, complex purification workflows, limited scalability, stringent Good Measuring Practice (GMP) standards requirements and sustainability targets. 

METTLER TOLEDO partners with peptide development teams, offering an integrated ecosystem of laboratory instruments and software solutions. This enables seamless process modeling, analytical data acquisition, cross platform data integration, bioprocess monitoring and control, manufacturing weighing and material control, packaging inspection and lifecycle services. Our solutions streamline processes, reduce variability, and support data-driven decisions across the entire peptide value chain.

Research Labs

Expand Analytical Coverage Without Expanding Complexity

Reduce Preparation Variability From the First Weigh-In

Pipette Like Your Data Depends on It

Standardize Execution, Not Just SOPs

Boost R&D throughput without losing comparability

Route Development

Scale Route Development Throughput With Automation

Standardize Route Execution and Data Management

Ensure Resin Performance and Efficient Linker Chemistry

Optimize Coupling and Cleavage Strategies

Optimize Cell Line Development for Recombinant Protein Production

Process Development 

Standardize Multi-Parameter Routines as Engineering Work Scales

Monitor Process Parameters With In-Line Sensors

Scale-up

See Process Changes in Real Time to Support Endpoint Decisions

In‑Lab QC

Make Routine QC Weighing Repeatable and Review-Ready

Meet Compendial UV/Vis Requirements With Traceable, Qualification-Ready Instruments

Reduce Transcription Risk With Connected, Standardized Workflows

Standardize Multiparameter QC Checks in One Workflow

Bioprocessing Monitoring & Control

Maintain pH Measurement Performance in Harsh Peptide Conditions

Stabilize Dissolved Oxygen Control During Dynamic Operation

Monitor Dissolved CO2 Frequently Enough for Control Decisions

Off-Line Process Checks

Standardize Key Unit Operations and Critical Parameters in Therapeutic Peptides Downstream Workflow

Optimize Formulation Development to Maintain Product Quality and Stability

Fast, in Situ Oxygen Safety Measurements in Small Spaces

From Raw Material to Final Fill: Weighing as the Critical GMP Control Point

Safe and Compliant Weighing in Hazardous and Hygienic Peptide Manufacturing Environments

The Critical Role of Gravimetric Control in Regulatory-Compliant Yield Management

Modular and Adaptable Weighing Solutions for Agile Biopharmaceutical Manufacturing

Scalable Weighing Solutions to Support Agile Production

Enhancing Peptide Production with Fully Integrated Weighing and Manufacturing Systems

Supporting the End-To-End Manufacturing Process

Packaging & Product Inspection

Detect Missing Parts in Multi-Component Peptide Packages

Handle Lightweight and Delicate Products at High Throughput Without Compromising Checks

Meet Stringent Compliance Requirements and Protect Product Integrity

Strengthen GLP‑1 Tablet Inspection From Infeed to Ship

Service: Lifecycle Support (Qualification, Training, Uptime)

Measure with Confidence and Accuracy

Calibration and Certificates

Achieve and maintain compliance through consistent procedures and adhere to local and global regulations and standards, such as:

1
ISO 17025
2
EURAMET
3
USP, GLP and GMP
4
NIST Handbook 44 and OIML
5
Measuring Instruments Directive (MID)
In Compliance with Your Quality System and Regulatory Standards

Equipment Qualification

Ensure a perfect start and ongoing, worry-free use with immediate and long-term benefits:

1
Assurance that the equipment is fit for use
2
Cost-savings through manufacturer's qualification services
3
Confidence that the equipment meets process requirements
4
Identification of needed calibration and maintenance
Boost Your Performance with Equipment Maintenance

Preventive Maintenance

Pre-plan your periodic maintenance that provides you with complete trust that your equipment achieves:

1
Consistent, accurate results
2
Safe and reliable operation
3
Optimal performance possible
4
A longer equipment lifespan, resulting in a higher ROI

Related Solutions for Peptide Therapeutics

Balancing Science and Process in Peptide Synthesis

Chemical Peptide Synthesis: Enhancing Yield and Purity

Biotechnological Peptide Production: Scale with Control

Buffer Preparation, Purification, Formulation, and Final Quality

Product Inspection: A Final Check for Patient Safety

What are the main steps in the peptide manufacturing process?

Peptide production relies on advanced biochemical synthesis using solid-phase peptide synthesis (SPPS) for short peptides, while for larger, more complex molecules requiring post-translational modification, bioprocesses using recombinant protein expression systems, or a combination of bioprocesses and biochemical synthesis are the system of choice to ensure purity, potency, and consistency.

How does solid-phase peptide synthesis (SPPS) build peptides step-by-step?​

1. A peptide is built step-by-step by adding amino acids in a precise sequence on a solid resin.

2. After each addition, excess chemicals are washed away and protective groups are removed to prepare for the next step.

3. The finished peptide is cleaved from the resin and purified, typically using HPLC.

4. The purified peptide is turned into a solid or liquid product. Quality control tests are run throughout to ensure purity, safety, and effectiveness.

What steps are involved in recombinant biological production of peptides?

1. Peptide-producing bacteria or yeast are grown in a nutrient-rich medium optimized for high yield.

2. Peptides are separated from the culture using centrifugation and filtration. If inside cells, the cells are broken open first.

3. Peptides are purified using techniques like chromatography and tangential flow filtration, followed by any necessary cleavage or modifications.

4. Excipients are added, and the product is tableted or filled into vials, under sterile conditions. Quality control tests ensure purity, safety, and functionality.

What are the key challenges in peptide synthesis?​

Chemical and solid phase peptide synthesis is a widely adopted method for peptide production, especially for short peptide production, and offers advantages over recombinant biological methods, in certain use cases: 

  • Cost: Manufacturing short peptides is less expensive at small to medium scale production, given simpler infrastructure requirements, fast turnaround time, and standardized resources. However, recombinant methods may be more cost-efficient at larger scales, longer or more complex peptides.

Whether produced through biochemical synthesis or recombinant biological methods, peptide manufacturing remains inherently expensive. Each approach comes with its cost drivers, from reagent and solvent use in chemical and solid-phase synthesis to complex infrastructure and long production cycles in biological expression. As a result, there is a strong drive across the industry to maximize process efficiency, minimize variability, and ensure consistent product quality at every scale.

  • Flexibility: It allows the incorporation of non-coding amino acids and diverse backbone modifications to improve stability.

  • Purity: Chemical and solid-phase synthesis methods avoid the risk of host-cell contaminants and enable precise control of the product. However, recombinant methods also achieve high purity with proper downstream processing.

What difficulties arise in biological peptide production methods?​

Recombinant biological approaches are common for larger proteins requiring complex post-translational modifications, and are advantageous for peptide production in circumstances such as:

  • Complexity: Biological methods enable complex peptide folding and specific post-translational modifications compared to chemical methods.

  • Sustainability: Chemical methods use an excess of high-purity, expensive reagents and solvents to ensure reaction completion, leading to greater chemical waste, and could affect global supply chains for essential solvents.

  • Peptide Length: Biological methods are better suited for producing longer peptides (>50 amino acids).

Process Analytics

製程水質檢測分析

純水分析控制生產過程

用於生物反應器的分析感測器

用於生物反應器的分析感測器

發酵及細胞培養中的精確製程控制

automated-reactor

Autochem 自動化學分析儀器

化學合成、製程開發與粒徑分析儀

dynochem biologics

Dynochem Biologics

Bioprocess Simulation Software

METTLER TOLEDO CytoDirect automated cell counter on a laboratory bench

Cell Counting

Instruments, Consumables, Software, and Service for Cell Counting

分析天平- 實驗室天平

分析天平

基礎秤重到高階應用一次滿足

METTLER TOLEDO precision balances

精密天平/精密電子秤

實驗室的精確秤重

梅特勒-托利多的紫外可見分光光度法

實驗室 UV-Vis 紫外/可見分光

儀器、附件、服務和軟體

實驗室酸鹼值儀器

pH計 (酸鹼度計)

酸鹼值和電導度測量解決方案

工業用磅秤與磅秤

工業稱重解決方案

支援 960Hz 高速數據處理與工業 4.0 自動化整合

產品檢測系統 | METTLER TOLEDO

經實證的產品檢測解決方案

檢查。保護。合規。

液體處理

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新的生命科學工具箱,在 3 個關鍵領域提供特定應用的知識及技巧:移液、分光光度法和 pH 測量。提高測量結果的可靠性並避免重複實驗。

細胞培養中的液體處理

細胞培養中的液體處理

《細胞培養中的液體處理》白皮書說明了可培養的不同類型細胞,以及每種類型細胞最適合的研究領域和工具。

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PAS-X MES 在製藥製造中的集成

稱重設備的集成對於合規性至關重要,柯爾柏與梅特勒-托利多的合作簡化了這一過程。

電子書封面

製藥稱重電子書

此電子書詳述了整個價值鏈中的產品,有助於確保製藥和生物製藥生產環境中的品質、效率和安全性。

藥物配方

藥物配方

高效、安全的藥物生產依賴於來自先進分析技術的可靠數據。配方優化和準確的 API 測量對於藥物的成功開發至關重要。

製藥行業智慧感測器管理 (ISM) 預測診斷工具指南

製藥行業的預測性診斷

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Four Pillars of Pharmaceutical Water Quality

製藥用水品質的四大支柱

在製藥行業,保持水的純度是一項堅定不移的承諾。深入研究電導率、TOC、生物負荷和臭氧的實時監測,以確保符合 USP 標準並保證藥物的安全性和有效性。

確保製藥用水合規性

確保製藥用水合規性

先進的水在線測量系統可確保藥品的安全和品質,同時滿足 PAT 和藥典要求。

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