

Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis
药品分析二极管阵列紫外可见分光光度计
- SKU UVI-0005
- UV-Vis
- CE (to be confirmed)
- IEC 61010-1 compliance (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Wavelength accuracy | ±1 nm |
| Spectral resolution | about 1–2 nm |
| Scan time | under 1 s full spectrum |
| Photometric range | –0.3 to 3.0 AU |
| Detector | Photodiode array |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <851>, USP <857>, USP <711>
What is the Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis?
A diode-array UV-Vis spectrophotometer captures a complete spectrum in under a second without scanning. It is chosen for method development, multi-wavelength measurements and the rapid screening of many samples in busy laboratories.
What is the Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis?
A diode-array UV-Vis spectrophotometer captures a complete spectrum in under a second without scanning. It is chosen for method development, multi-wavelength measurements and the rapid screening of many samples in busy laboratories.
Overview
A diode-array spectrophotometer disperses light after it has passed through the sample and images the whole spectrum onto a photodiode array, so all wavelengths are recorded simultaneously. There are no moving parts in the wavelength selection, which makes measurements fast and mechanically robust, and spectra can be captured in under a second. This suits method development, where full spectra reveal the best wavelength and the shape of absorption bands, and it supports multi-component analysis and kinetic measurements at several wavelengths at once. Spectra can be stored and compared with libraries, and peak purity or ratio calculations are possible. Photometric range and stray light are usually slightly inferior to a good double-beam instrument, so it is often used alongside one for routine high-accuracy assay.
How does it work?
A UV-Vis spectrophotometer passes light from a deuterium lamp, for ultraviolet, and a tungsten or halogen lamp, for visible, through a monochromator and then through a sample. Transmitted intensity is compared with that through a reference to give absorbance, which follows the Beer-Lambert relationship when the absorbing species, path length and wavelength are fixed. Concentration is calculated from absorbance using a calibration curve or an absorptivity value. In pharmaceutical work the sample is usually a diluted solution or a filtered dissolution aliquot held in a quartz or matched glass cell. Absorbance range, wavelength accuracy, stray light, spectral bandwidth and cell path length determine the usable range, and the method defines the wavelength, blank and standard procedure.
What are the key features?
- Simultaneous recording of the full spectrum
- No moving parts in wavelength selection
- Spectra captured in under a second
- Multi-wavelength and kinetic measurements
- Spectral storage and library comparison
- Rapid screening of many samples
What are the technical specifications?
A typical diode-array uv-vis spectrophotometer for pharmaceutical analysis configuration offers wavelength range of 190–1100 nm, wavelength accuracy of ±1 nm, spectral resolution of about 1–2 nm, scan time of under 1 s full spectrum, photometric range of –0.3 to 3.0 AU and detector of Photodiode array. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis is used in method development and screening, multi-component colorimetric analysis, reaction kinetics monitoring and rapid sample screening. Across the wider UV-Vis class, laboratories also deploy it for pharmaceutical assay, content uniformity testing and dissolution monitoring.
Which standards and certifications apply?
Relevant standards and methods include USP <851>, USP <857>, USP <711>, USP <905>, ICH Q2(R2) and IEC 61010-1. Certification candidates for this model are CE, IEC 61010-1 compliance and ISO 13485 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the instrument on a stable bench away from direct sun and draughts, and allow the lamps to warm up and stabilise before measurement. Use matched cells of the specified path length and check them for scratches and contamination, because a mismatched cell introduces a constant error. Verify wavelength accuracy and photometric accuracy at defined intervals with certified reference materials, and record the results. Prepare solutions accurately and measure within the validated absorbance range, since high absorbance reduces linearity. Replace lamps when energy falls, and keep cells clean and stored properly. Retain raw spectra and calibration data for regulatory inspection.
How do I select the right Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis?
Choose a diode-array instrument for method development, multi-wavelength work, kinetics or sample screening, where full spectra in one shot are valuable. Confirm spectral resolution, wavelength accuracy and photometric range for your application, and keep a double-beam or high-accuracy instrument for routine release assay if photometric precision is critical.
How does it compare with other UV-Vis variants?
Choose the spectrophotometer from the method and the sample workload. Single-beam instruments suit routine assay at a fixed wavelength, where cost and simplicity matter. Double-beam optics compensate for lamp drift and are preferred for stability-indicating methods, wavelength scans and long runs. Diode-array instruments capture a full spectrum quickly, which helps method development and multi-wavelength work. For dissolution monitoring, dedicated fibre-optic systems measure absorbance directly in the vessel. Compare wavelength range and accuracy, photometric range and noise, cell changer capacity and warm-up stability. Confirm that the instrument can be qualified with standards such as potassium dichromate or holmium oxide filters, and that software supports audit trails.
Full specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Wavelength accuracy | ±1 nm |
| Spectral resolution | about 1–2 nm |
| Scan time | under 1 s full spectrum |
| Photometric range | –0.3 to 3.0 AU |
| Detector | Photodiode array |
| Cell positions | 1–8 with sipper |
| Power supply | 220 V, 50 Hz, about 0.2 kW |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Method development and screening
- Multi-component colorimetric analysis
- Reaction kinetics monitoring
- Rapid sample screening
Key features
- Simultaneous recording of the full spectrum
- No moving parts in wavelength selection
- Spectra captured in under a second
- Multi-wavelength and kinetic measurements
- Spectral storage and library comparison
- Rapid screening of many samples
Frequently asked questions about Diode-Array UV-Vis Spectrophotometer for Pharmaceutical Analysis
Light that passes through the sample is dispersed by a grating and projected onto an array of photodiode detectors, each covering a narrow wavelength band. All wavelengths are measured at once, so a full spectrum needs no scanning motion.
Photometric range and stray light are typically a little inferior to a well-designed double-beam spectrophotometer, which matters at high absorbance. For absorbance values in the usual working range the difference is small and often negligible for routine analysis.
Recording a full spectrum shows the maxima and band shape, which guides wavelength selection and reveals whether the analyte and matrix overlap. Comparing spectra across a peak or across samples checks specificity and detects changes such as degradation.
Absorbance is proportional to the concentration of the absorbing species and the path length, at a fixed wavelength. This linear relationship allows concentration to be calculated from measured absorbance, provided the solution is dilute and no interfering species absorb.
Wavelength accuracy is checked with holmium oxide or didymium filters, photometric accuracy with potassium dichromate or neutral density filters, and noise and stray light are verified by the manufacturer's procedure. Checks are repeated at defined intervals and after service.
Absorbance depends on path length and the optical quality of the cell. Unmatched or scratched cells add a constant error to every reading, which can shift results even when the chemistry is correct, so cells should be paired and inspected regularly.
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