DrotaverineHydrochlorideChecker

Drotaverine Hydrochloride Quality Checker

Lumex QC URS & FS input.csv output.json rule-based LIMS-ready API
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Utility description: Drotaverine Hydrochloride Quality Checker

Drotaverine Hydrochloride Quality Checker — Drotaverine Hydrochloride (No-Spa)

ℹ️  Utility checks critical parameters of Drotaverine Hydrochloride API:
    • Assay (99.0–101.0%)
    • Impurity A (papaverine-related) ≤0.5%
    • Impurity B (other isoquinolines) ≤0.5%
    • Loss on drying ≤0.5%
    • Residue on ignition ≤0.1%
    • pH of solution (3.0–4.5)
    • Heavy metals ≤10 ppm
    • Chloride content (9.5–10.5%)

⚠️  IMPORTANT: Drotaverine is an isoquinoline antispasmodic.
    Control of related alkaloids (papaverine) is critical for safety.
    Exceeding impurities may increase cardiovascular side effects.

Usage:
  DrotaverineHydrochlorideChecker.exe                            → demo mode (console output)
  DrotaverineHydrochlorideChecker.exe input.csv output.json      → evaluate your data

Input format:
BatchNumber,AssayPercent,ImpurityAPercent,ImpurityBPercent,LossOnDryingPercent,ResidueOnIgnitionPercent,pH_Solution,HeavyMetalsPPM,ChlorideContentPercent

Example:
  DROT-HCL-2026-005,99.8,0.15,0.10,0.25,0.05,3.8,5,10.1

— WHY IS THIS NEEDED?
Drotaverine Hydrochloride is a myotropic antispasmodic, PDE IV inhibitor.
• Widely used in gastroenterology, urology, and gynecology.
• Requires strict control of related compounds (synthesis from papaverine or similar precursors).
• Hygroscopicity requires loss on drying control.

⚠️  CRITICAL:
• Assay 99.0–101.0% — ensures therapeutic efficacy.
• Impurity A (papaverine-related) ≤0.5% — toxicological limit.
• Impurity B (other isoquinolines) ≤0.5% — synthesis completeness control.
• pH 3.0–4.5 (1% solution) — indicator of correct salt formation.
• Chlorides 9.5–10.5% — confirmation of hydrochloride stoichiometry.

Key features:
• Check of specific isoquinoline impurities.
• Chloride ion content control for salt confirmation.
• Hygroscopicity assessment (LOD).
• Full LabWare LIMS compatibility.

Critical parameters:
• Assay: 99.0–101.0%
• Impurity A: ≤0.5%
• Impurity B: ≤0.5%
• Loss on Drying: ≤0.5%
• Residue on Ignition: ≤0.1%
• pH (1% sol): 3.0–4.5
• Heavy Metals: ≤10 ppm
• Chlorides: 9.5–10.5%

💡 Usage tips:
1. Impurities controlled by HPLC with UV detection (240-250 nm).
2. Chloride content determined by argentometry (silver nitrate titration).
3. Loss on drying determined by drying at 105°C.
4. pH measured in freshly prepared 1% aqueous solution.

⚠️ Note: Drotaverine is structurally similar to papaverine. The method must clearly separate these two compounds, as papaverine is the main potential contaminant/impurity of synthesis.

input.csv

BatchNumber,AssayPercent,ImpurityAPercent,ImpurityBPercent,LossOnDryingPercent,ResidueOnIgnitionPercent,pH_Solution,HeavyMetalsPPM,ChlorideContentPercent
DROT-HCL-2026-005,99.8,0.15,0.10,0.25,0.05,3.8,5,10.1
DROT-HCL-2026-006,98.5,0.60,0.20,0.30,0.08,4.2,8,10.0

URS & FS — User Requirements and Functional Specification

This document defines the controlled interface, validation behaviour and expected output of DrotaverineHydrochlorideChecker. The document is intended to reside inside the utility folder together with input.csv and the description file. Expected executable: DrotaverineHydrochlorideChecker.exe.

Purpose: the utility performs deterministic verification of QC input data against approved limits, generates machine-readable output.json, and supports QC/QA review, LIMS/ELN/MES integration and CSV/CSA preparation.

Scope

Utility classHPLC / chromatographic QC
Main object/methodDrotaverine Hydrochloride (No-Spa)
Inputinput.csv with a fixed header and controlled data types.
Outputoutput.json with PASS, WARNING, FAIL statuses, detailed checks and critical findings.
ExclusionsThe utility does not replace the approved specification, analytical procedure, OOS/OOT investigation or Qualified Person / QA release decision.

Domain limits and critical parameters

Key fragments from the source description are listed below. Before production use, limits shall be verified against the approved specification, registration dossier, current pharmacopoeial edition and local SOPs.
  • • Assay (99.0–101.0%)
  • • Impurity A (papaverine-related) ≤0.5%
  • • Impurity B (other isoquinolines) ≤0.5%
  • • Loss on drying ≤0.5%
  • • Residue on ignition ≤0.1%
  • • pH of solution (3.0–4.5)
  • • Heavy metals ≤10 ppm
  • • Chloride content (9.5–10.5%)
  • ⚠️ IMPORTANT: Drotaverine is an isoquinoline antispasmodic.
  • DrotaverineHydrochlorideChecker.exe input.csv output.json → evaluate your data
  • BatchNumber,AssayPercent,ImpurityAPercent,ImpurityBPercent,LossOnDryingPercent,ResidueOnIgnitionPercent,pH_Solution,HeavyMetalsPPM,ChlorideContentPercent
  • • Widely used in gastroenterology, urology, and gynecology.
  • • Requires strict control of related compounds (synthesis from papaverine or similar precursors).
  • • Hygroscopicity requires loss on drying control.
  • ⚠️ CRITICAL:
  • • Assay 99.0–101.0% — ensures therapeutic efficacy.

Production data flow

StepResponsible objectDescriptionControl
1LIMS/ELN/MES or QC analystCreates input.csv with measured values and batch identifier.Header, mandatory-field and unit checks.
2DrotaverineHydrochlorideCheckerLoads CSV, converts data types, applies domain rules and produces the result.Deterministic rules; no ML/probabilistic conformance decision.
3QC reviewer / QAReviews output.json, warnings, critical deviations and source values.Review, deviation investigation and data-trail retention.
4Archive / eQMSRetains input, output, utility version, documentation and checksum.Data integrity: ALCOA+, reproducibility and change control.

URS — User Requirements Specification

IDRequirementCriticalityAcceptance criterion
URS-001The utility shall be supplied with DrotaverineHydrochlorideChecker.documentation.html in the same folder as the description and sample input.csv.MediumThe documentation file exists in the DrotaverineHydrochlorideChecker folder and opens locally in a browser.
URS-002The utility shall accept input.csv with the exact headers defined in the data contract.HighA CSV file with the correct header is processed without manual editing.
URS-003The utility shall validate mandatory fields, column count, data types and basic plausibility of values.HighSchema and conversion errors are explicitly reported.
URS-004The utility shall evaluate each critical and non-critical QC parameter against approved limits.HighEach checked parameter receives a status and explanatory message.
URS-005The utility shall produce a final record/batch status: PASS, WARNING or FAIL.HighA critical deviation causes FAIL; a non-critical deviation causes WARNING.
URS-006The utility shall generate output.json suitable for LIMS/ELN/MES integration and QA/QC review.HighJSON contains source values, rules, statuses, warnings and critical findings.
URS-007The utility shall preserve traceability between batch identifier, input values, applied rules and final status.HighThe output contains the batch/row identifier and list of checked parameters.
URS-008The utility shall not use machine learning or probabilistic interpretation for conformance decisions.MediumThe result is reproducible and based on explicit rules, thresholds and input values.
URS-009The utility shall support the CLI scenario: DrotaverineHydrochlorideChecker.exe input.csv output.json.HighWith valid arguments, output.json is created; on error, a diagnostic message is returned.
URS-010The documentation shall support IQ/OQ/PQ or equivalent CSV/CSA verification.MediumThe document contains URS, FS, CSV contract, rules, test scenarios and traceability.
URS-011The utility shall distinguish data errors, method warnings and critical specification failures.Highoutput.json provides separate structures/fields for errors, warnings and critical findings.
URS-012The utility shall support archival retention of unchanged input and output data.Mediuminput.csv and output.json can be retained as a batch record or OQ/PQ evidence.

input.csv contract

#FieldTypeSamplePurpose
1BatchNumberstringDROT-HCL-2026-005Batch or lot identifier used for traceability.
2AssayPercentdecimal99.8Assay/content result used to verify quantitative compliance.
3ImpurityAPercentdecimal0.15Purity parameter; used for conformance, impurity and release assessment.
4ImpurityBPercentdecimal0.10Purity parameter; used for conformance, impurity and release assessment.
5LossOnDryingPercentdecimal0.25Water/moisture or loss-on-drying parameter relevant for stability and quality.
6ResidueOnIgnitionPercentstring0.05Controlled input parameter used by the deterministic QC rules.
7pH_Solutiondecimal3.8Solution pH; relevant for stability, compatibility and administration.
8HeavyMetalsPPMdecimal5Elemental impurity / residual metal parameter.
9ChlorideContentPercentstring10.1Concentration/content value controlled against the specification.
BatchNumber,AssayPercent,ImpurityAPercent,ImpurityBPercent,LossOnDryingPercent,ResidueOnIgnitionPercent,pH_Solution,HeavyMetalsPPM,ChlorideContentPercent
DROT-HCL-2026-005,99.8,0.15,0.10,0.25,0.05,3.8,5,10.1
DROT-HCL-2026-006,98.5,0.60,0.20,0.30,0.08,4.2,8,10.0

Input validation rules

IDFieldTypeCheckCriticality
VR-001BatchNumberstringnot empty; unique within file where applicableMedium
VR-002AssayPercentdecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved % limitHigh
VR-003ImpurityAPercentdecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved % limitHigh
VR-004ImpurityBPercentdecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved % limitHigh
VR-005LossOnDryingPercentdecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved % limitMedium
VR-006ResidueOnIgnitionPercentstringnot empty where mandatoryMedium
VR-007pH_Solutiondecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved numerical limitHigh
VR-008HeavyMetalsPPMdecimalparse as invariant decimal; finite value; no NaN/Infinity; evaluate against approved numerical limitHigh
VR-009ChlorideContentPercentstringnot empty where mandatoryHigh

FS — Functional Specification

IDFunctionImplementationURS link
FS-001Local HTML documentationProvide a bilingual DrotaverineHydrochlorideChecker.documentation.html file with RU/EN switch, source description, URS, FS, contracts and tests.URS-001, URS-010
FS-002CSV importRead input.csv in UTF-8/CSV-compatible format and identify the header row and data records.URS-002, URS-009
FS-003Schema validationCompare actual columns against the expected contract; missing key fields are recorded as schema errors.URS-002, URS-003
FS-004Type conversionConvert decimal, flag/boolean and controlled string values. Invalid values are recorded at row and field level.URS-003
FS-005Domain rule engineApply rules for Drotaverine Hydrochloride Quality Checker, including critical limits from the description and approved specification.URS-004, URS-008
FS-006Status aggregationAggregate parameter statuses: FAIL for critical failure, WARNING for non-critical deviation, PASS for conformance.URS-005, URS-011
FS-007JSON exportWrite output.json with utility identifier, source values, check results, warnings and critical findings.URS-006, URS-007
FS-008Error handlingSeparate execution errors, schema errors, conversion errors and domain-limit failures.URS-003, URS-011
FS-009Audit supportKeep result structure suitable for review, OOS/OOT investigation, calculation reproduction and inspection discussion.URS-007, URS-012
FS-010Integration contractSupport the standard scenario: LIMS/ELN/MES creates input.csv, the utility returns output.json, and the portal displays description and documentation.URS-006, URS-009
FS-011Configuration/change controlAny change to limits, column names or rule logic requires versioning, review, regression tests and documentation update.URS-010, URS-012
FS-012Data integrityDo not modify the source input.csv; save results separately in output.json for archival retention.URS-007, URS-012

Example output.json structure

{
  "utilityId": "drotaverinehydrochloridechecker",
  "utilityName": "DrotaverineHydrochlorideChecker",
  "object": "Drotaverine Hydrochloride Quality Checker",
  "overallStatus": "PASS|WARNING|FAIL",
  "sourceFile": "input.csv",
  "recordCount": 2,
  "checks": [
    {
      "parameter": "BatchNumber",
      "value": "DROT-HCL-2026-005",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-001"
    },
    {
      "parameter": "AssayPercent",
      "value": "99.8",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-002"
    },
    {
      "parameter": "ImpurityAPercent",
      "value": "0.15",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-003"
    },
    {
      "parameter": "ImpurityBPercent",
      "value": "0.10",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-004"
    },
    {
      "parameter": "LossOnDryingPercent",
      "value": "0.25",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-005"
    },
    {
      "parameter": "ResidueOnIgnitionPercent",
      "value": "0.05",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-006"
    },
    {
      "parameter": "pH_Solution",
      "value": "3.8",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-007"
    },
    {
      "parameter": "HeavyMetalsPPM",
      "value": "5",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-008"
    },
    {
      "parameter": "ChlorideContentPercent",
      "value": "10.1",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result",
      "ruleReference": "VR-009"
    }
  ],
  "criticalFindings": [],
  "warnings": [],
  "metadata": {
    "executionMode": "CLI",
    "interface": "CSV to JSON",
    "documentationFile": "DrotaverineHydrochlorideChecker.documentation.html"
  }
}

Traceability matrix URS → FS → OQ/PQ

URSFSVerificationExpected result
URS-001FS-001Check that DrotaverineHydrochlorideChecker.documentation.html exists in the utility folder.The file exists, opens, and the RU/EN switch works.
URS-002/003FS-002/003/004Run the utility with a correct CSV, a CSV missing a mandatory column and a CSV with an invalid data type.Correct CSV is processed; schema and type errors are explicit.
URS-004/005FS-005/006Submit values within limits, at warning level and beyond a critical limit.PASS, WARNING and FAIL are produced according to rules.
URS-006/007FS-007/009/012Verify output.json structure and batch traceability.JSON contains batch identifier, values, rules, statuses and critical findings.
URS-008FS-005Repeat execution with the same input.csv.The result is identical; no probabilistic behaviour is present.
URS-009/010/012FS-010/011/012Execute the CLI scenario and archive input/output/version.Artefacts are suitable for OQ/PQ and change-control records.

OQ/PQ test scenarios

IDScenarioInput dataExpected result
OQ-001Positive pathSample CSV with valid values.output.json is created; final status is PASS or acceptable WARNING according to rules.
OQ-002Mandatory column missingRemove one key column from the header.Schema error; the row shall not be treated as passed.
OQ-003Invalid typePut text into a numeric field.Type-conversion error with field and row identification.
OQ-004Critical limitCritical parameter value outside the approved limit.FAIL and an entry in criticalFindings.
OQ-005WarningNon-critical deviation or unknown controlled category.WARNING without hiding the source value.
PQ-001User real batchReal input.csv from the QC process.Reviewed result with input.csv, output.json, version and checksum retained.

QA/QC, CSV/CSA and change control

  • Do not rename columns without updating the validator, test set and documentation.
  • Retain input.csv, output.json, executable version, checksum and a copy of the documentation.
  • Before production use, perform IQ/OQ/PQ or equivalent risk-based CSV/CSA verification.
  • Critical limits shall be approved by the process owner and verified against the registration dossier, pharmacopoeia and local SOPs.
  • Any change to rules, thresholds or status interpretation shall go through change control and regression testing.

Included in packages

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Gastroenterology QC Suite

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Gynecology QC Suite

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