SDIP: SEMEN-DERIVED INJECTION PROTOCOL

iblamethebrain

iblamethebrain

Maxillofacial Surgical Assistant
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SDIP — SEMEN-DERIVED INJECTION PROTOCOL

Subcutaneous + Intramuscular Auto-derived Molecular Augmentation

The first biologically closed-loop system for hormonal, aesthetic, and neuroregenerative enhancement.


1/ ABSTRACT:

Semen is a nutrient-dense, proteomic biofluid, evolutionarily designed to deliver epigenetically-modified payloads across hostile environments. It contains exosomes, microRNAs, immunomodulators, and trace concentrations of neuromodulatory and endocrine molecules. This thread explores the design of SDIP—a protocol for harvesting, purifying, and reintegrating semen-derived compounds via injection, bypassing digestive degradation and enabling targeted systemic effects.



——


2/ PHILOSOPHY OF SDIP:
• Semen is not waste. It’s the final form of cellular synthesis—epigenetically tuned, rich in biologically active compounds.
• Most of its components are destroyed through oral consumption.
• The body treats it as disposable only because reproduction externalizes it. SDIP inverts that logic—you keep what you produce
• You are your own drug.


3/ COMPOSITION OF SEMEN (per ejaculate, ~3.4ml):


ComponentFunctionalityNotes
Zinc (12–15 mg/L)5α-reductase inhibition, skin repairHigh bioactivity
Fructose (200–300 mg/ejaculate)Cellular fuelMetabolically dense
Prostaglandins (PGE1, PGE2, PGF2α)Vasodilation, inflammation modulationPossible tissue remodeling
Oxytocin (trace)Bonding, mood elevationSub-perceptual dose
Exosomes (~10⁸–10⁹/ml)Intercellular signalingCan carry mRNA, miRNA
TGF-β, IL-10Immunosuppressive cytokinesMay downregulate inflammation
Basic fibroblast growth factor (bFGF)Angiogenesis, tissue growthPossible skin enhancement
DNA/RNA fragmentsEpigenetic carriersOrigin-specific

The goal of SDIP is to retain, isolate, and reintroduce only the bioactive components above in therapeutically useful concentration.


4/ PROTOCOL STAGE I – COLLECTION & PRE-STORAGE:

• Ejaculate via standard masturbation, no lube (contaminants).
• Use sterile collection vial (borosilicate or medical-grade plastic).
• Immediately chill to 4°C.
• Freeze within 30 min using controlled-rate freezing (-80°C ideal, domestic freezer tolerable for early experimentation).
• Label with timestamp. No pooling across days (epigenetic variance).


5/ PROTOCOL STAGE II – FRACTIONATION & FILTRATION:

A. Thaw & Dilute:

• Rapid thaw in 37°C water bath.
• Dilute 1:1 with sterile phosphate-buffered saline (PBS).

B. Centrifugation:
• Spin at 3000g for 15 min.
• Pellet = spermatozoa (discard).
• Supernatant = seminal plasma (retain).

C. Microfiltration:

• Pass through 0.22μm filter to remove bacteria and large particulates.
• Optional: Use Amicon Ultra centrifugal filters (3kDa cutoff) to isolate peptides/exosomes from metabolic waste.

D. Sterilization (Chemical):
• Optional ethanol vapor exposure (70%) OR UV irradiation.
• Note: Both risk denaturing bioactive peptides—experimental discretion required.


6/ PROTOCOL STAGE III – STORAGE & DOSING FORMULATION:

• Lyophilize (freeze-dry) filtered extract for stable long-term storage.
• Reconstitute in 1ml bacteriostatic saline per dose (subQ) OR 2ml (IM).
• Dosing interval: every 7–14 days.
• Injection site rotation recommended.
• No adjuvants unless immunotolerance confirmed.

7/ INJECTION MODALITIES:
Subcutaneous (SubQ)

• Goal: systemic distribution, low absorption curve.
• Use 0.5ml insulin syringe, 27–31G needle.
• Inject into abdominal fat or thigh.


Intramuscular (IM):

• Goal: higher bioavailability, possible localized tissue interaction.
• 1.0–2.0ml volume.
• Use 23–25G needle, ventrogluteal or deltoid site.


8/ THEORETICAL PATHWAYS OF ACTION:


TargetMechanismOutcome
HPG AxisEndogenous signal peptides may modulate GnRH/LH↑ Testosterone stabilization
Skin MatrixProstaglandins + bFGF stimulate fibroblasts↑ Collagen, ↓ acne inflammation
NeurochemistryOxytocin + dopamine microdoses↑ Mood, ↓ stress response
Immune SystemExosomal miRNA may dampen autoimmunity↓ Chronic inflammation
MusculatureAndrogenic trace moleculesPossible hypertrophy assistance



9/ SAFETY PROFILE (THEORETICAL):

• No live cells
• Autologous origin = low rejection risk
• Contamination risk = moderate unless lab-grade precautions used
• Immune response: unlikely if filtered, but test with microdose first
• Long-term effects: completely unknown (you are the guinea pig)


10/ THE VISION:

Semen isn’t waste. It’s the distilled informational essence of your biological being.
Through SDIP, you become closed-loop. You reclaim what’s yours.
You don’t inject testosterone—you inject your genomic whisper.
You’re not enhancing. You’re reconverging.


END/ Future stages may include:
• Topical microneedling with seminal exosome serum
• Intranasal microdose delivery
• Direct exosome cloning & modification
• Codifying sperm bioactivity signatures into a biological passport



This is SDIP v0.1.

Not yet tested. Not yet optimized.

But when the first human runs this to full cycle and logs outcomes?
Not sure.
 
  • +1
Reactions: Sonneillon
SDIP — SEMEN-DERIVED INJECTION PROTOCOL

Subcutaneous + Intramuscular Auto-derived Molecular Augmentation

The first biologically closed-loop system for hormonal, aesthetic, and neuroregenerative enhancement.


1/ ABSTRACT:

Semen is a nutrient-dense, proteomic biofluid, evolutionarily designed to deliver epigenetically-modified payloads across hostile environments. It contains exosomes, microRNAs, immunomodulators, and trace concentrations of neuromodulatory and endocrine molecules. This thread explores the design of SDIP—a protocol for harvesting, purifying, and reintegrating semen-derived compounds via injection, bypassing digestive degradation and enabling targeted systemic effects.



——


2/ PHILOSOPHY OF SDIP:
• Semen is not waste. It’s the final form of cellular synthesis—epigenetically tuned, rich in biologically active compounds.
• Most of its components are destroyed through oral consumption.
• The body treats it as disposable only because reproduction externalizes it. SDIP inverts that logic—you keep what you produce
• You are your own drug.


3/ COMPOSITION OF SEMEN (per ejaculate, ~3.4ml):


ComponentFunctionalityNotes
Zinc (12–15 mg/L)5α-reductase inhibition, skin repairHigh bioactivity
Fructose (200–300 mg/ejaculate)Cellular fuelMetabolically dense
Prostaglandins (PGE1, PGE2, PGF2α)Vasodilation, inflammation modulationPossible tissue remodeling
Oxytocin (trace)Bonding, mood elevationSub-perceptual dose
Exosomes (~10⁸–10⁹/ml)Intercellular signalingCan carry mRNA, miRNA
TGF-β, IL-10Immunosuppressive cytokinesMay downregulate inflammation
Basic fibroblast growth factor (bFGF)Angiogenesis, tissue growthPossible skin enhancement
DNA/RNA fragmentsEpigenetic carriersOrigin-specific

The goal of SDIP is to retain, isolate, and reintroduce only the bioactive components above in therapeutically useful concentration.


4/ PROTOCOL STAGE I – COLLECTION & PRE-STORAGE:

• Ejaculate via standard masturbation, no lube (contaminants).
• Use sterile collection vial (borosilicate or medical-grade plastic).
• Immediately chill to 4°C.
• Freeze within 30 min using controlled-rate freezing (-80°C ideal, domestic freezer tolerable for early experimentation).
• Label with timestamp. No pooling across days (epigenetic variance).


5/ PROTOCOL STAGE II – FRACTIONATION & FILTRATION:

A. Thaw & Dilute:

• Rapid thaw in 37°C water bath.
• Dilute 1:1 with sterile phosphate-buffered saline (PBS).

B. Centrifugation:
• Spin at 3000g for 15 min.
• Pellet = spermatozoa (discard).
• Supernatant = seminal plasma (retain).

C. Microfiltration:

• Pass through 0.22μm filter to remove bacteria and large particulates.
• Optional: Use Amicon Ultra centrifugal filters (3kDa cutoff) to isolate peptides/exosomes from metabolic waste.

D. Sterilization (Chemical):
• Optional ethanol vapor exposure (70%) OR UV irradiation.
• Note: Both risk denaturing bioactive peptides—experimental discretion required.


6/ PROTOCOL STAGE III – STORAGE & DOSING FORMULATION:

• Lyophilize (freeze-dry) filtered extract for stable long-term storage.
• Reconstitute in 1ml bacteriostatic saline per dose (subQ) OR 2ml (IM).
• Dosing interval: every 7–14 days.
• Injection site rotation recommended.
• No adjuvants unless immunotolerance confirmed.

7/ INJECTION MODALITIES:
Subcutaneous (SubQ)

• Goal: systemic distribution, low absorption curve.
• Use 0.5ml insulin syringe, 27–31G needle.
• Inject into abdominal fat or thigh.


Intramuscular (IM):

• Goal: higher bioavailability, possible localized tissue interaction.
• 1.0–2.0ml volume.
• Use 23–25G needle, ventrogluteal or deltoid site.


8/ THEORETICAL PATHWAYS OF ACTION:


TargetMechanismOutcome
HPG AxisEndogenous signal peptides may modulate GnRH/LH↑ Testosterone stabilization
Skin MatrixProstaglandins + bFGF stimulate fibroblasts↑ Collagen, ↓ acne inflammation
NeurochemistryOxytocin + dopamine microdoses↑ Mood, ↓ stress response
Immune SystemExosomal miRNA may dampen autoimmunity↓ Chronic inflammation
MusculatureAndrogenic trace moleculesPossible hypertrophy assistance



9/ SAFETY PROFILE (THEORETICAL):

• No live cells
• Autologous origin = low rejection risk
• Contamination risk = moderate unless lab-grade precautions used
• Immune response: unlikely if filtered, but test with microdose first
• Long-term effects: completely unknown (you are the guinea pig)


10/ THE VISION:

Semen isn’t waste. It’s the distilled informational essence of your biological being.
Through SDIP, you become closed-loop. You reclaim what’s yours.
You don’t inject testosterone—you inject your genomic whisper.
You’re not enhancing. You’re reconverging.


END/ Future stages may include:
• Topical microneedling with seminal exosome serum
• Intranasal microdose delivery
• Direct exosome cloning & modification
• Codifying sperm bioactivity signatures into a biological passport



This is SDIP v0.1.

Not yet tested. Not yet optimized.

But when the first human runs this to full cycle and logs outcomes?
Not sure.
wtf is baby shitley telling these greys

'inject your semen' :lul:
 
  • +1
  • JFL
Reactions: truechadpreet, Norwegian LTN and iblamethebrain
such a good theory yet only hate
 
  • +1
Reactions: iabsolvejordan
I understand now why normies call us gay
 
  • +1
Reactions: iblamethebrain
I understand now why normies call us gay
No. This is peak health. Eating semen is close, but digestion kills it. So go intramuscular or SubQ.
 
@realshit bisogno una cosa da te....
 
i'll inject my semen into your ass boy
 
  • +1
Reactions: iblamethebrain
Bookmarking for research-purposes… interesting theory, will dive deeper later
 
  • +1
Reactions: iblamethebrain
Bookmarking for research-purposes… interesting theory, will dive deeper later
Thanks for not being semen = ew.

Im not sure if we have any current scientific understanding of how it could be beneficial. Maybe im leaning into a bit of a esotheric territory, but i just can‘t accept to think that there is nothing hypervaluable in the literal life essence.

I think trying it would be cool and insightful. I dont see any great immediate risk. Just potential time wasted, but thats always the trade off in scientific research.
 
  • +1
Reactions: iabsolvejordan

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