Growth kinetics and process timing. Fast, clear, and lab-ready.
PulseGrowth is a lightweight web app for analyzing cell growth kinetics and estimating process timing in mammalian cell culture workflows.
It is part of Host Cell, a growing suite of practical laboratory and bioprocess tools built by Emiliano Balderas (IBt-UNAM).
PulseGrowth helps convert routine sampling data into actionable bioprocess metrics for mammalian cell culture.
The app is organized into three practical modules:
- Bio-Kinetics: calculates growth metrics from two sampling points
- Metabolics (q): estimates qGlc and qGln normalized by IVCD
- Feed Control: estimates simple feed additions to restore target concentrations
It is designed for quick bench-side calculations, passaging decisions, and culture monitoring.
PulseGrowth uses an exponential growth model between two sampling points:
- X0: initial viable cell density (typically in ×10⁶ cell/mL)
- X1: final viable cell density (typically in ×10⁶ cell/mL)
- Δt: elapsed time between measurements
- μ: specific growth rate
PulseGrowth calculates:
To normalize metabolite consumption rates, PulseGrowth estimates Integrated Viable Cell Density (IVCD) as:
This is useful for obtaining more comparable specific rates (q) than using only initial or final cell density.
This section explains exactly how the app performs the calculations.
Given X0, X1, and Δt:
- Convert Δt to a common internal time basis (hours, if needed)
- Compute μ using the exponential growth equation
- Compute doubling time from μ
- Compute expansion factor = X1/X0
- Compute IVCD for downstream q calculations
PulseGrowth estimates specific metabolite rates using concentration change normalized by IVCD.
If the user enters metabolite concentrations in g/L, the app converts them internally to mM using molecular weight (MW):
Default MW values used:
- Glucose (Glc) = 180.156 g/mol
- Glutamine (Gln) = 146.145 g/mol
If the user enters values directly in mM, no conversion is needed.
For each metabolite:
Where:
- C0 = initial concentration
- C1 = final concentration
Positive ΔC means net consumption.
PulseGrowth reports q values consistently in pmol/cell/day:
Where:
- ΔC is in mM
- IVCD is in (10^6\ cell\cdot h)/mL
- The factor 24 converts from per-hour to per-day basis
PulseGrowth estimates the feed volume required to adjust a metabolite concentration from current to target level using a single-addition correction formula.
For a feed stock concentration Cstock, current concentration Ccurrent, target concentration Ctarget, and culture volume Vculture:
This is a simple algebraic planner for practical lab use, not a full dynamic feeding model.
PulseGrowth uses a unit strategy designed for consistency and comparability.
- Expected in ×10⁶ cell/mL
- hours or days
- Internally normalized for growth-rate calculations
- g/L or mM (for Glc / Gln)
- Primary output: pmol/cell/day
- Optional display: pg/cell/day (mass-equivalent reference)
PulseGrowth ensures q outputs are comparable by converting g/L → mM internally before calculation.
✅ This means:
- entering glucose as 6 → 4 g/L
- or entering equivalent values in mM
...will produce comparable qGlc values (aside from rounding), because the app normalizes units before computing q.
- Growth Kinetics Solver: Calculates μ, doubling time, and expansion factor
- IVCD-Based q Estimation: qGlc / qGln normalized using exponential IVCD approximation
- Unit-Aware Metabolite Inputs: Accepts g/L or mM and converts internally
- Simple Feed Planner: Quick feed-volume estimates for glucose and glutamine correction
- Time Input Flexibility: Manual Δt or start/end datetime input
- Mobile-First UI: High-contrast, telemetry-inspired interface for real lab use
- PWA Ready: Installable on Android/iOS and usable offline after first load
- Host Cell Design System: Visual consistency with other tools in the suite
PulseGrowth is useful for:
- estimating whether a culture is still in exponential growth
- comparing growth performance across clones or conditions
- calculating doubling time for passaging planning
- estimating qGlc and qGln from routine sampling data
- planning simple corrective feeds for glucose/glutamine
- reducing manual calculator/transcription errors during culture operations
- Enter X0, X1, and Δt
- Select time unit (h or day)
- Click Analyze kinetics
- Review μ, t_d, expansion factor, and IVCD
- Enter Glc and/or Gln concentrations as C0 → C1
- Select units (g/L or mM)
- Click Calculate q
- Review qGlc and qGln in pmol/cell/day
- Enter culture volume
- Enter stock concentrations and target concentrations
- Click Calculate feed plan
- Review estimated feed volumes
PulseGrowth can be installed as a Progressive Web App (PWA) for faster access and offline use.
- Open the live app
- Tap/click Install App (if shown)
- Or use the browser install prompt/menu
- Open the live app
- Tap Share
- Select Add to Home Screen
Once installed, the app can work offline after the required files are cached.
Q: Why does PulseGrowth convert g/L to mM for q calculations?
A: Because q should be comparable across inputs. Concentration changes in g/L and mM are not directly equivalent without using molecular weight (MW). PulseGrowth converts to mM internally before computing q.
Q: What does a positive q mean?
A: By convention in PulseGrowth, q > 0 means net consumption (C0 > C1). Negative q means the metabolite increased over time (net accumulation/production).
Q: Is IVCD exact?
A: No. The app uses an exponential approximation of IVCD between two sampling points. It is practical and useful for routine comparisons, but still depends on the underlying growth behavior and data quality.
Q: Does this replace process models or SOPs?
A: No. PulseGrowth is a calculation aid for rapid workflow support. Always validate decisions against SOPs, process knowledge, and experimental context.
- PulseGrowth is a calculation aid, not a substitute for SOPs or experimental judgment.
- Exponential assumptions may not hold if the culture is in lag/stationary/decline phase.
- IVCD is an approximation based on two sampling points.
- Feed calculations are simplified and intended for quick operational estimates.
- Always verify:
- units and concentration basis
- sampling times
- viable cell count quality / counting consistency
- stock solution identity and concentration
- For critical workflows, follow institutional protocols and lab-specific validation practices.
Emiliano Balderas
Biotechnology Engineer | PhD Student in Biochemistry
Instituto de Biotecnología (IBt) - UNAM
Host Cell is a growing suite of practical lab and bioprocess tools focused on:
- clarity
- speed
- reproducibility
- real-world usability at the bench
PulseGrowth is one module in that ecosystem.
Host Cell Lab Suite – Practical tools for high-performance biotechnology.