The Challenges of Preparing Accurate Sample and Standard Concentrations

Making the Switch to Gravimetric Solution Preparation

天秤に関するUSP第41章および第1251章

天秤に関するUSP第41章および第1251章

最新改訂2025 / 2026への準拠を確実なものに

詳細はこちら

METTLER TOLEDO's Solution for Accurate Solution Preparation with Automated Solvent Dispensing

XPR自動分注天秤

See How You Can Benefit from Automated Solvent Dispensing: An Application Example

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HPLC向け参照用標準液

アプリケーションノート: 標準液の正確な調製(日本語版)

このアプリケーションノートでは、HPLCや他のクロマトグラフィ(分析)メソッド向けに正確な参照用標準液を調製するためのすばやく簡単な方法について説明します。

残留農薬試験 – 正確な標準試料作製

残留農薬検査 – 正確な標準試料作製

食品、農産物、動物飼料の残留農薬試験は、世界の食品安全規制で義務付けられています。正確な標準試料の調製は、残留物が限界を下回っている検査に不可欠です。

微量金属分析

費用対効果の高い微量金属分析

微量金属分析では微量の金属を定量します。 そのような潜在的な毒性を持つ元素不純物の分析では、サンプルと参照用標準を正確に計量する必要があります。

手作業と重量法によるサンプル調製の比較

重量法によるサンプル調製を始めるべき10の理由

手作業によるサンプル調製時に発生するエラーの潜在的な原因に関するガイドをダウンロードしてください。重量法を使用すべき10の理由をご確認ください。

第一三共社におけるサンプル調製

第一三共株式会社におけるサンプル調製

このケーススタディでは、第一三共株式会社が、クアントス自動粉体・液体分注の導入により、分析用サンプル調製の所要時間とコストをいかに節約したかについて解説しています。

Frequently Asked Questions

What is gravimetric sample preparation?

Gravimetric sample preparation is weighing the sample, either manually or automated, and then delivering the required amount of solvent to achieve the desired concentration. The solvent amount is calculated automatically based on the actual amount of sample weighed, and measured by weight. Gravimetric dosing is referenced in USP chapter 1251 Weighing on an analytical balance as a type of weighing typically used for sample or standard preparation.

How can I prepare stock solutions more efficiently?

A major advantage of automated systems is that without the need of a human operator. This allows to extend the working time of your lab to 24h a day.

How can I ensure that my standard solutions are traceable?

Standard solutions are traceable when prepared on the XPR Automatic Balance because the amount of standard weighed and the amount of solvent added is recorded automatically. The resulting concentration is also calculated automatically. This information, along with all relevant metadata, is stored electronically or exported as required, making the standard preparation process fully traceable.

How can I ensure that all the steps in my analytical procedures meet compliance regulations or guidelines?

If you consider USP requirements for analytical weighing and data integrity by following the ALCOA+ framework, it is important to ensure that the balance you are using is appropriate for the amount you need to weigh out. You must respect the minimum weight specification and keep within the safe weighing range for your laboratory environment. The GWP Approved function on the XPR Automatic Balance will show you whether the minimum weight requirement is adhered to or not. For data management, the powder weighed is identified by the RFID chip in the dosing head to avoid errors, and the weight dispensed into each vial is recorded automatically and can be exported with all necessary metadata if required using LabX laboratory software. All this data is included in the audit trail for full compliance with regulations.

How do I switch from concentrations from mg/ml to mg/g?

A concentration in mg/g can be converted to mg/ml, and vice versa, using a simple density conversion (density = mass/volume). However, if a standard calibration curve is generated in mg/ml to start with, then the conversion is unnecessary because the sample concentration is measured relative to the calibration curve. 

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