

Automated Cell Block Processor
自动细胞块处理机
- SKU CYP-0004
- Cytology Processors
- 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
| Samples per run | 1–12 |
|---|---|
| Minimum cell number | about 50–100 cells per block |
| Coagulant option | Plasma and thrombin, agar or matrix |
| Cycle time | about 2–4 h including processing |
| Block size | Standard cassette |
| Reagent exchange | Automated |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61010-2-101, IEC 61326-1
What is the Automated Cell Block Processor?
An automated cell block processor concentrates residual cells from a cytology sample into a paraffin block that can be sectioned. It is chosen when immunohistochemistry or molecular testing must be performed on cytology material.
What is the Automated Cell Block Processor?
An automated cell block processor concentrates residual cells from a cytology sample into a paraffin block that can be sectioned. It is chosen when immunohistochemistry or molecular testing must be performed on cytology material.
Overview
A cell block turns loose cells into a tissue-like block that can be sectioned and stained by the same methods used in histology. The processor centrifuges residual sample, sometimes after adding a coagulant such as plasma and thrombin, agar or a commercial matrix, then fixes, dehydrates and infiltrates the pellet with paraffin. The resulting block yields multiple sections for hematoxylin and eosin, immunohistochemistry and molecular assays, which is valuable when the cytology sample is the only material available or when a cell block avoids a repeat biopsy. Automated processors standardise the pelleting, reagent exchange and embedding steps, improving cell recovery and reducing hands-on time. Cell yield depends strongly on the number of cells in the original sample, so samples with very few cells may still give an inadequate block.
How does it work?
A cytology processor starts with a sample collected into a preservative solution, which fixes cells and lyses red blood cells. The instrument then separates diagnostically useful cells from mucus, blood and inflammatory debris using one of several approaches. Density gradient or centrifugation methods layer the sample over a reagent so cells of interest band at a known density. Filtration and membrane methods trap cells on a surface with a defined pore size, then transfer them to a slide. Some platforms use an adhesive or charged coating to capture cells while washing away the rest. The result is a thin, evenly distributed preparation with cells concentrated in a defined area, which improves screening speed and reduces obscuring material. Cell recovery, spot area and carryover control determine performance.
What are the key features?
- Concentration of residual cells by centrifugation
- Optional coagulant or matrix to bind the pellet
- Automated fixation, dehydration and paraffin infiltration
- Sections suitable for immunohistochemistry
- Standardised reagents and step timing
- Multiple sections from one block
What are the technical specifications?
A typical automated cell block processor configuration offers samples per run of 1–12, minimum cell number of about 50–100 cells per block, coagulant option of Plasma and thrombin, agar or matrix, cycle time of about 2–4 h including processing, block size of Standard cassette and reagent exchange of Automated. 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 Automated Cell Block Processor is used in immunohistochemistry on cytology samples, molecular testing on cytology material, effusion and aspirate cell blocks and ancillary testing without repeat biopsy. Across the wider Cytology Processors class, laboratories also deploy it for cervical cancer screening, urine cytology and body fluid cytology.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61010-2-101, IEC 61326-1, ISO 15189 and CLSI GP41. 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.
Place the processor on a stable bench near a drain and power outlet, and keep the working area free of clutter so sample tubes can be tracked. Follow the specified reagent volumes and incubation or centrifugation conditions, because under-processing leaves debris while over-processing loses cells. Change reagents and clean fluid paths on schedule to prevent contamination and biofilm. Verify performance with control samples and record reagent lot numbers, run dates and results. Train staff in safe handling of preservative fluids, which may contain methanol or other hazardous substances, and dispose of waste according to local regulations.
How do I select the right Automated Cell Block Processor?
Specify a cell block processor when cytology samples must support immunohistochemistry or molecular testing, or when residual fluid should be archived as a block. Confirm minimum cell yield, coagulant options, cycle time and block format. Very scant samples may not yield a usable block regardless of the instrument.
How does it compare with other Cytology Processors variants?
Choose a processor by sample type, throughput and whether the laboratory prefers an open or closed reagent system. For high-volume cervical screening, a liquid-based processor with automated staining and coverslipping gives the most consistent results. For body fluids and fine-needle aspirates, a centrifugation or filter-based method often yields better cell recovery from scant samples. Cell block processors support immunohistochemistry and molecular testing on residual cells. Compare samples per run, reagent consumption, carryover prevention, consumable cost and whether the platform accepts third-party reagents. Confirm validation, training and service support, and check that the output format fits existing stainers and coverslippers.
Full specifications
| Samples per run | 1–12 |
|---|---|
| Minimum cell number | about 50–100 cells per block |
| Coagulant option | Plasma and thrombin, agar or matrix |
| Cycle time | about 2–4 h including processing |
| Block size | Standard cassette |
| Reagent exchange | Automated |
| Section thickness | 3–5 µm on a microtome |
| Power supply | 220 V, 50 Hz, about 0.3 kW |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Immunohistochemistry on cytology samples
- Molecular testing on cytology material
- Effusion and aspirate cell blocks
- Ancillary testing without repeat biopsy
Key features
- Concentration of residual cells by centrifugation
- Optional coagulant or matrix to bind the pellet
- Automated fixation, dehydration and paraffin infiltration
- Sections suitable for immunohistochemistry
- Standardised reagents and step timing
- Multiple sections from one block
Frequently asked questions about Automated Cell Block Processor
A block can be sectioned and stained by standard histology methods, so immunohistochemistry, special stains and molecular tests are possible. It also provides archival material and can avoid a repeat biopsy when cytology is the only sample.
Roughly 50 to 100 cells as a minimum for a usable block, though more is better for multiple tests. Samples with very few cells may give sections without representative material, so cytology and cell block results are usually interpreted together.
Plasma with thrombin, agar or a commercial matrix binds loose cells into a firm pellet that survives processing and sectioning. Without a coagulant, sparse cells can be lost during reagent exchange. The choice depends on the downstream tests.
It prepares a cell sample from liquid suspension into a slide-ready monolayer. It removes mucus, blood and debris, concentrates diagnostically useful cells and deposits them in a defined area so the microscopist can screen the slide quickly and reliably.
The sample is rinsed into a preservative fluid rather than smeared directly onto a slide. The processor then removes debris and deposits a representative cell population as a thin monolayer, which usually improves cell distribution and reduces obscuring blood and mucus.
Filter methods trap cells on a membrane with a defined pore size and transfer them to a slide, while centrifugation methods concentrate cells by density. Filtration generally gives cleaner preparations, and centrifugation often recovers more cells from very scant samples.
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