Data Input
Load concentration-time data via file upload, manual entry, or Smart Parse.
File Upload / Manual Entry
Smart Parse
InstantPaste anything — CSV, Excel table, JSON, or even a text description of your data. The AI will extract time-concentration pairs automatically.
Data Preview
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Analysis Configuration
Configure NCA parameters. Linear-up Log-down trapezoidal method with Best Fit λz selection.
Dosing Information
Calculation Method
Ascending: linear trapezoid. Descending (both C > 0): log-linear trapezoid. C=0: linear fallback.
Automated selection of terminal phase regression points using maximum adjusted R² criterion. Minimum 3 points, post-Tmax, C > 0, negative slope required.
Computed Parameters:
NCA Results
Complete pharmacokinetic parameter estimates.
Primary PK Parameters
Run analysis to see results.
Terminal Phase Regression (λz)
Run analysis to see terminal phase details.
Interval Data (AUC/AUMC Buildup)
Run analysis to see interval data.
PK Profile Visualization
Concentration-Time Profile
Terminal Phase Residuals
Validation & Benchmarks
Unit tests against published reference values using the Theophylline Subject 1 standard dataset.
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Methodology Reference
Linear-up Log-down Rule
Ascending (Ci+1 ≥ Ci):
AUC = (Ci + Ci+1) / 2 × Δt
Descending (Ci+1 < Ci, both > 0):
AUC = (Ci − Ci+1) / (ln Ci − ln Ci+1) × Δt
Zero concentration: Linear trapezoidal fallback
Best Fit λz Algorithm
- Identify Tmax (last occurrence if multiple Cmax)
- Consider only post-Tmax points with C > 0
- For n = 3 to N terminal points, perform OLS on ln(C) vs t
- Require: slope < 0, adjusted R² ≥ 0.80
- Select: maximum adjusted R², then maximum n (tiebreaker)
References
- Gabrielsson J, Weiner D. Pharmacokinetic & Pharmacodynamic Data Analysis. 5th ed. 2016.
- Rowland M, Tozer TN. Clinical Pharmacokinetics and Pharmacodynamics. 4th ed. 2010.
- FDA Guidance for Industry: Bioanalytical Method Validation. 2018.