PROJECT PULSE: LAB JOURNAL 01

Page 1

E.A.S .E .


E.A.S.E

PROJEC T PULS E_ _


NOTE: TH I S J O URN A L I S TH E P RO P E RTY OF TH E E X P E RI M E N TA L A S S O C IATION FO R S CI E N TI FI C E VO LUTI O N(E . A. S. E)

DATE:

21.01.2310

All experiments were conducted within our laboratories with the exclusion of studies conducted in facilities overseas.

All research and experiments were done under the strict supervision and approval of the team leads of PULSE.


E.A.S.E

21. 01. 2310

CLAUSES A N D R E G U L AT I O N S 1. This journal is to remain in the records vault of the E.A.S.E headquarters unless requested to be brought out for referencing purposes. The journal is not to be brought back to personal living quarters or offices. 2. All information, research and recordings in this journal are not to be breached or shared with outside parties, including close acquaintances and family members. Leakage of information will be traced and dealt with by the chief officers of E.A.S.E. 3. All members involved in the contribution of this journal are to understand the risks and precautions involved and are to abide with the agreements stated. 3. All experiments and tests are to be conducted within the facilities of E.A.S.E unless given permission under special circumstances. 4. All experiments and tests are to be recorded and tagged with their subsequent code numbers. Secret experimentations will lead to severe consequences. 5. Routine checks will be conducted frequently to ensure the lab journals are at their place in the vault. Missing journals will be reported immediately and traced. 6. Any personel suspected to attempt a leakage of information or experimentations done in secrecy are to be reported immediately. 7. All members involved in the contribution of this project are not allowed to back out until the completion of the project except under special circumstances.


CONTENT

CONTENT

ABOUT E.A.S.E.

01

PULSE TEAM

02

OVERVIEW

03

TIMELINE

05

PAST RESEARCH AND STUDIES

07

STUDY: HUMAN BLOOD AND PLASTICS

09

EQUIPMENT AND MACHINE CHECK-01

11

T E S T - T 0 1 A N D A N A LY S I S

13

T E S T - T 0 2 A N D A N A LY S I S

18

T E S T - T 0 3 A N D A N A LY S I S

25

EQUIPMENT AND MACHINE CHECK-02

33

SUBJECTS PROFILE

35

SUBJECT MONITOR

37


E.A.S.E

ABOUT E.A.S.E

The Ex pe rime n ta l A s so c i at i o n Fo r S c i e n t i f i c Evolution (E. A. S. E) w as e st ab l i s he d i n 2 07 0 by a g roup of sci en tis ts th a t w i s he d t o m ake a c h an ge i n t h e evolut ion of ma n kin d t hro u g h d ar i n g e x p e r i m ent a t ions . In 2088 , d ue to our v i si o n of ac hi e v i n g m o re a nd t h e di ffere n ce s be twe en o u r go al s, E .A .S .E l e f t t h e U nit ed S ci ence N a tion a n d fo r m e d o u r ve r y o w n g ro u nd s and pr a ctice s . Sin ce t h e n , w e have b e e n co n d uct ing experime n ts on our o w n an d have c am e u p w i t h va rious new i n ve n tion s a n d c u re s t hat has g re at ly b e nef it ed t owards h e a lth ca re an d t he e co n o m y. Movi n g forwa rd, E. A .S .E p l an s t o co n t i n u e b e i ng a revolu tion a ry force i n t he s c i e n t i f i c f i e l d w i t h our b old t ri als a n d re s e a rch , e ve n i f w e are f ace d w i t h ris ks a nd cri t i cis m tow a rd s o u r p r ac t i ce s fo r t h e g re at e r good .

01


TEAM

‘PULSE’ TEAM LEADS

RESEARCHERS

DR J. WARNEY HEAD OF L A B O R ATO R Y A N D E X P E R I M E N TAT I O N S

PROFFESOR DOFF DIVISION OF MEDICAL SCIENCES

DR H. SOO HEAD OF HUMAN STUDIES

MS REINKE DIVISION OF HUMAN STUDIES

SCIENTISTS

O P E R AT O R S

DR DINAH HEAD OF MEDICAL SCIENCES

MS HELENA HEAD OF EQUIPMENT AND MACHINERIES

D R N AT HEAD OF M AT E R I A L R E S E A R C H DR RUGHON HEAD OF MOLECULAR M O D I F I C AT I O N S

M R W. R AY DIVISON OF EQUIPMENT AND MACHINERIES

02


E.A.S.E

21. 01. 2310

OVERVIEW: PROJECT PULSE THE STUDY OF SYNTHETIC HUMAN BLOOD REPLACEMENT

INTRODUCTION

Since the beginning of heathcare, there has long been a need for blood substitutes when it comes to the human body. Look at the problems we have faced with human blood—people who die from excessive bleeding in accidents, issues with blood transfusions, donated blood having a short shelf-life, etc. With our increasing population growth and vast advancement in science and technology, it is even more apparent for us to act now and attempt a revolutionary invention that could change the whole field of medical sciences. With the concerns that were mentioned before, the study of a blood replacement has thus been a crucial research subject for scientists and doctors alike, and there has been attempts in developing substitues for the human blood. This is of course no easy feat and records have shown that this is an effort that had started all the way back in the 1600s.

REFERENCE: Suman Sarkar, Artificial blood (2008) Indian J Crit Care Med; 12(3): 140–144.DOI: 10.4103/0972-5229.43685

03

The types of blood substitutes attempted include the usage of milk, animal blood, crystal salt solutions and several chemical solvents. However, they were all deemed not suitable as they all still had a short shelf-life and loses its blood-like functions over time. The closest finding to a breakthrough came in the 2000s, where researchers found a substitute by merging plastics in blood, thus promising a replacement that will last longer.


OVERVIEW

However, with the technological tools available at that time, the project could not continue and the study was thus abandoned. With the techonological advancements of today, E.A.S.E was inspired to reopen this study again and has recently discovered a new form of plastic compound that holds close resemblance to that of the human blood composition. The potential of this discovery thus led to the project PULSE, aimed at the research and development of this new compound as a blood substitute.

OBJECTIVES

The new synthetic blood developed in PULSE should ideally fulfill the following requirements. The blood should be compatible with the human body and suitable for blood transfusions, no matter the blood type of the human carrier. The new blood should not raise any contamination issues or viruses, which means it would have to be a recognisable substance to the white blood cells. The blood must of course be able to perform the functions of human blood or more, such as transporting oxygen throughout the bloodstreams and releasing carbon dioxide when necessary. The visocity and solubilty of the new blood will also have to be considered as it should flow well through the blood vessels and eliminate the risk of blood clotting. Apart from that, the new blood should have a shelf-life of 6 months and above, an improvement from normal blood which can only be stored for 1. The newly developed blood will go through several tests and trials before it is ready to be tried on human subjects. The ultimate goal of course, would be to experiment the usage of the developed PULSE blood on the human body so as to produce a more concrete outcome and hypothesis. The subjects will then be monitored for over a year to check whether the new blood is functioning well in their bloodstreams as well as to study the effects of the PULSE blood on their bodies. If successful, the new blood will enter the second stage of mass development. .

SIGNED BY

DR J WARNEY

DR H SOO

JW

HS 04


E.A.S.E

TIMELINE E S T I M AT E

21.01.2310

15.03.2310 —31.06.2310

PROJECT PULSE COMMENCES

FURTHER TESTS A N D A N A LY S I S

05

24.01.2310

01.03.2310

EQUIPMENT CHECK AND TESTING 01

TEST 01 OF FIRST PULSE SAMPLE

2 7. 0 1 . 2 3 1 0 —28.02.2310

0 1 . 07. 2 3 1 0

P R E PA R AT I O N AND FURTHER RESEARCH

FINAL VERSION OF PULSE TO BE DEVELOPED


TIMELINE

01.08.2310 EXPERIMENTS ON TEST SUBJECTS

01.01.2311 —31.12.2311 MONITORING OF TEST SUBJECTS

01.01.2312 PHASE 1 END

01.11.2310 T E S T R E S U LT S A N D A N A LY S I S

EXPECTED DEADLINE

01.2312

(PHASE 1)

ACKNOWLEDGED BY E.A.S.E AND THE TEAM OF PULSE

06


E.A.S.E

PAST RESEARCH AND STUDIES

YR 2007

‘SHEFFIELD SCIENTISTS DEVELOP ARTIFICIAL BLOOD’

DEPARTMENT OF CHEMISTRY

10 MAY 2007

UNIVERSITY OF SHEFFIELD, UNITED KINGDOM

Scientists from the University of Sheffield are developing an artificial 'plastic blood', which could act as a substitute for real blood in emergency situations. The 'plastic blood', which will be on display at the Science Museum this month, could have a huge impact on military applications. Because the artificial blood is made from a plastic, it is light to carry and easy to store. Doctors could store the substitute as a thick paste in a blood bag and then dissolve it in water just before giving it to patients – meaning it’s easier to transport than liquid blood.

ARCHIVED

Donated blood has a relatively short shelf-life of 35 days, after which it must be thrown away. It also needs refrigeration, whereas the ‘plastic blood’ will be storable for many more days and is stable at room temperature.

Fig 01. Excerpt 01 of Sheffield Scientist develop ‘Artificial blood’.

07


PAST STUDIES

The artificial blood is made of plastic molecules that hold an iron atom at their core, just like haemoglobin, that can bind oxygen and could transport it around the body. The small plastic molecules join together in a tree-like branching structure, with a size and shape very similar to that of natural haemoglobin molecules. This creates the right environment for the iron to bind oxygen in the lungs and release it in the body.

Fig 02. Excerpt 02 of Sheffield Scientist develop ‘Artificial blood’.

While still in its development, the scientists hope this will make it particularly useful for military applications and being plastic, it’s also affordable. The scientists are now seeking further funding to develop a final prototype that would be suitable for biological testing. Dr Lance Twyman, from the Department of Chemistry at the University of Sheffield and who has been developing the artificial blood for the last five years, said: “We are very excited about the potential for this product and about the fact that this could save lives.

Fig 03. Excerpt 03 of Sheffield Scientist develop ‘Artificial blood’

SOURCE: ‘Sheffield Scientist develop Artificial blood’ (2007),University of Sheffield. Retrieved from: https://www.sheffield.ac.uk/news/nr/808-1.175169

08


E.A.S.E

23. 01. 2310

STUDY: HUMAN BLOOD AND PLASTICS THE FUNCTION OF BLOOD IN HOMOSAPIENS.

ABSTRACT

clot parts of blood to heal wounds or attack harmful bacteria that enters the body.

This is a summarised version of the research and findings the team has done in preparation for this project.

The components of the blood are made up of the red blood cells(erythrocytes), white blood cells(leukocytes), platelets, and the plasma. Further breaking down the components of the blood will lead us to proteins, which includes the plasma-proteins, as well as the the metalloprotein, haemogloblin. This iron substance as we all know, is responsible for the oxygen-carrying function in blood.

Keywords: Blood, plastics, synthetic blood.

The blood is a lifesaving fluid or tissue that is present all around the human body. Many also call it an organ since it performs crucial functions that helps keep the body working. Its numerous functions includes of course, transporting oxygen and removing carbon dioxide from the bodily cells. Besides the circulatory tract, blood also helps with the digestive system by transporting nutrients and waste from the intestines and the kidneys. The components present in blood also have protective properties, where they

09

When it comes to blood transfusion, one should note that the haemoglobin level should be 13.5 g/dl or more and weigh more than 65 kg. The platelet count should be 150,000/mm3 or more, the white cell count and differential count should be within normal limits although the synthetic blood developed with PULSE should only mainly replace the properties and functions of the red blood cells.


STUDY

Plastics on the other hand, which in this case, the thermoplastic, polyethylene, is a light-weight and durable polymer that has been manufactured and popularly used in the 2000s as a form of material for numerous packaging or living quarters neccessities.

E.A.S.E finally reached a breakthrough when we developed a new composite polymer that was found to have a composition similar to the red blood cells of the existing human blood(Figure 01), though it still needs more research to reach a concrete consensus.

The polymer has a number of high-performing properties, such as its toughness, chemical inertness, low coefficient friction as well as low electrical conductivity. Most importantly, it has a particularly versatile and mallaeble molecular crystalline structure, allowing the polymer to morph and adapt into whichever form it is needed for.

This study shows us the potential of this project in producing synthetic blood and this brings us one step closer to our goals. There were also clarifications made about the precautions the team will have to make while prepping for the future development and trials of the new blood substance.

Through the years, polyethylene has since been developed for various other applications outside of just being a material. It wasn’t until recently that we discovered a new lead that could allow it to branch onto medical science. While E.A.S.E was researching on plastics as candidates for the blood substitutes, we saw a potential in the adaptable property of polyethylene. We modified the polymer to fulfill certain qualities. The result will need to have coupling agents that would attach the polymer to blood substances, forming strong covalent bonds instead of Van der Waals.

OH

H

O

O

O

O x

Fig 04. Molecular composition of Human Blood.

SOURCES 01. Debdatta Basu, Rajendra Kulkarni (2014), Overview of blood components and their preparation, Indian J Anaesth.58(5): 529–537. DOI: 10.4103/0019-5049.144647

02. P. Noorunnisa Khanam, Mariam Al Ali AlMaadeed (2015) Processing and characterization of polyethylenebased composites, Advanced Manufacturing: Polymer & Composites Science, 63-79 DOI: 10.1179/2055035915Y.0000000002

10


E.A.S.E

EQUIPMENT AND MACHINES USED

EQUIPMENT CHECKED AND TESTED BY MS HELENA

HC 24. 01. 2310

MAIN PROCEDURES:

MIXING OF BLOOD A N D P O LY E H T H Y L E N E E X A M I N AT I O N A N D D O C U M E N TAT I O N UNDER MICROSCOPE

VCH MICROSCOPE

11


EQUIPMENT CHECK-01

EVANS MIXER

X M - X LV H 1

12


E.A.S.E

B ATC H 0 1 TEST CODE: L125 01. 03. 2310

T E S T­-T 0 1 DESCRIPTION:

The first batch of PULSE blood was developed by the Laboratories of E.A.S.E using a fusion of the new polymer composite and components from the plasma of human blood. A sample from the batch was tested and analysed. Key analysis includes molecular structure, solubility and compatability with the human body.

MACHINES AND EQUIPMENT USED:

TRANSFUSIONER VCH MICROSCOPE X M - X LV H 1 EVANS MIXER

Fig 05. Sample from Batch 01 of PULSE, Date: 01. 03. 2310.

13


TEST-T01

Fig 06. Close-up cellular view of Sample L125, Date: 01. 03. 2310.

Fig 07. Substance view of Sample L125, Date: 01. 03. 2310.

14


E.A.S.E

Fig 08. Microscopic composition of PULSE Sample 01—Magnifiedx20, Date: 01. 03. 2310.

15


TEST-T01

Fig 09. Microscopic composition of PULSE Sample 01—Magnifiedx50, Date: 01. 03. 2310.

REMARKS: Sample L125 shows a more ‘plastic-ish’ composition than a bloodlike composition. The outcomes are too blur and unclear to determine the inner structure or solubility of the sample. This could be due to an uneven mixture of the blood and the poly material during fusion. More dosage of haemogloblin mix is to be issued to the next sample. Analysis of the sample will not be continued till clearer results are produced. Better, much efficient equipment will have to be used as well. Request for magnification at x200 for the next batches of tests.

DR H.SOO 03. 03. 2310

16


E.A.S.E

SAMPLE L125

5 0 % M ATC H

HUMAN BODY

*PULSE will only be subjected to tests on human subjects when data match reaches 85% and above.

17


TEST-T02

B ATC H 0 2 TEST CODE: L235 09. 04. 2310

T E S T­-T 0 2 DESCRIPTION:

The second batch of PULSE blood developed by the Laboratories of E.A.S.E. The dosage of leukocytes and haemoglobin was increased in this batch of samples. A sample from the batch was tested and analysed. Key analysis includes molecular structure, solubility and compatability with the human body.

MACHINES AND EQUIPMENT CHANGE:

XM3000 USED INSTEAD OF XM-LXVH1 M A G N I F I C AT I O N INCREASED TO X200

Fig 10. Sample from Batch 02 of PULSE, Date: 09. 04. 2310.

18


E.A.S.E

Fig 11. Microscopic composition of PULSE Sample 02—Magnifiedx20, Date: 09. 04. 2310. 19


TEST-T02

Fig 12. Microscopic composition of PULSE Sample 02—Magnifiedx200, Date: 09. 04. 2310. 20


E.A.S.E

D ATA A N AY L S I S

15. 04. 2310

20

15

L235 AVERAGE

COMPOSITION— NEW COMPOUNDS:

10

P O LY A L K Y L E N E 05

HAPTOGLOBIN FLUOROCARBON P O LY E T H Y L E N E

00

00

02

05

Fig 13. Units of RBC duplicated in Sample L235.

RECORDED BY MS REINKE

RC

21

The total amount of RBC was increased in the new blood sample, allowing the haemoglobin to transport oxygen more efficiently. The erythrocytes concentration is nearly as close, though the addition of polyalkylene and polyethylene binds the blood thickness more tightly and would result in the release of lesser oxygen to the body tissue and individual cells.


TEST-TO2

SAMPLE L235 COMPOSITION

O H

H

O HUMAN BLOOD COMPOSITION

O

OH

H

O

O

O

O x

M AT C H I N G COMPOUNDS:

A—OXYGEN B—CHLORIDE C—HYDROGEN D—HAEMOGLOBIN E — P O LY S A C C H A R I D E

The study of the composition of sample L235 in comparision with that of the human blood shows its structural similarities and we filtered out their matching compounds. This is a promising outcome, although just for precautionary measures, the following compounds input should be increased in accordance to the percentages present below.

A 10%

B 23%

C 22%

D 10%

E 22%

22


E.A.S.E

C O M PATA B I L I T Y D I A G R A M

23

R A D I AT I O N D I S TA N C E S

SOLUBILITY: 0.025MOL/L

3.2

AT O M I C RADIUS

PH7

RADIAL SIZING

50%

AT O M I C RADIUS-2


TEST-T02

SAMPLE L235

7 0 % M ATC H

HUMAN BODY

*PULSE will only be subjected to tests on human subjects when data match reaches 85% and above.

24


E.A.S.E

B ATC H 0 3 TEST CODE: L436 15. 05. 2310

T E S T­-T 0 3 DESCRIPTION:

The third batch of PULSE blood developed by the Laboratories of E.A.S.E. The dosage of erythrocytes, polysaccharide and chloride was increased in this batch of samples. A sample from the batch was tested and analysed. Key analysis includes polypeptide studies and compatability with the human body.

MACHINES AND EQUIPMENT XM3000 M A G N I F I C AT I O N S T I L L AT X 2 0 A N D X 2 0 0

Fig 14. Sample from Batch 03 of PULSE, Date: 15. 05. 2310.

25


TEST-T03

Fig 15. Microscopic composition of PULSE Sample 03—Magnifiedx20, Date: 15. 05. 2310.

26


E.A.S.E

Fig 16. Microscopic composition of PULSE Sample 03—Magnifiedx200-1, Date: 15. 05. 2310.

27


TEST-T03

Fig 17. Microscopic composition of PULSE Sample 03—Magnifiedx200-2, Date: 15. 05. 2310.

28


E.A.S.E

30. 05. 2310

D ATA - O 3 A N AY L S I S P O LY P E P T I D E CHAIN SEQUENCES:

A — P O LY A L K Y L E N E B—HAPTOGLOBIN C—FLUOROCARBON D — P O LY E T H Y L E N E E — P O LY S A C C H A R I D E

49% A

55% B

65% C

80% D

49% E

L E V E L S O F P O LY P E P T I D E S E Q U E N C E S

Human erythrocyte membranes were boiled and dissolved to determine the molecular weights of the constituent proteins. The process realases the polypeptide chains labelled A, B , C ,D and E which we measured and tried to duplicate into the new PULSE sample. The cells’ recgonitive properties will register the new substances as amino acids substitutes.

Fig 18. New protein structure.

29


DATA-03

PROTEIN AND AMINO ACID SEQUENCES IN SAMPLE L436 PRESENTED IN A DITHER DIAGRAM:

___________________________________MHOO1 3 HOFNA2

Z LOU

A34

3 MCHOA1

TRIY78

00 AA

A35

XX GLOU

LYSA6

8 THR

A6

9 SERA7

VALA9

11 LYS

A9

12 THRA10

LEUA12

14 TRP

A12

LYSA15 4 VALC1

3 SOR

-7 ASP

B1

C3

-37 TRPC4

39 THR

OX

40 ARGC7

42 TYR

B7

38 MHOO1

69 GLYE14

65 ALA

E14

70 ALAE15

72 SERE17

68 ASN

E17

-73 ASPE18

75 LEUE20

71 ALA

APF

PHE

GH5

122 MHOO1

XX1

H9

129 LEU GLYH15

TYR

O H15

135 VAL

142 ALAH21 HO2

127 LYS

134 VALH13

132 VAL

139 ASNH18 H20

118 THR

131 GLNH10 H12

GH3

145 TYRHC3

H10

H13

141 ARG

125 LEU 128 PHE

135 ALAH14

133 SER

H16

136 LEU

143 HISHC1 HC3

GH4

1

H19 139 LYS

A14

39 GLNC6

17

41 THR

64 ASP

XXX

67 THR

E16

70 VAL

-121 GLUGH5 H8

E19 1 87

130 TYRH9

H11

131 SER

133 VALH12 H14

138 ALAH17 141 LEUH20 HC1

14

38 THR

74 GLYE19

116 GLU

132 LYSH11

140 ALAH19 H21

E18

11

A11

16 LYS

71 PHEE16

129 ALAH8

137 VALH16

138 SER

V15

8

A8

36 PROC3 C5

-1

A4

13 ALA

68 LEUE13

69 ALA

120 LYSGH4

130 ALA

H18

E12

90 LPU

H1

O2

40 LYS

41 PHECE1

XXX XXX

10 VAL

16 GLYA14

37 PRO

NB2

56 ILS

13 ALAA11

A30

35 TYRCI

1 OAL

45 THRA2

10 ALAA8

A11

15 GLY

SDA1

7 MCHOA1

A4

12 ALA

B4

A2

A3

9 ASN

15 TRPA13

36 PHE

CH1 NAL

136

134 THR

H17

137 THR

144 LYSHC2

140

IXX X_____________________________

30


E.A.S.E

SAMPLE L436

9 2 % M ATC H

HUMAN BODY

T H I S S A M P L E I S S U I TA B L E F O R T E S T S A N D E X P E R I M E N TAT I O N S ON HUMAN SUBJECTS.

31


TEST-T03

REMARKS:

With the switch of equipment and x200 magnification, we were successful in capturing the desired outcomes in samples L235 and L436. In L235, we could already make out some blood cell-like features present in the PULSE sample and with x200 magnification, we were able to zoom in on the modified red blood cells and see the polyethylene composite binding the substances together. This was a promising result and we ran it for data analysis. After some rectifications, we came up with the new batch L436 in Test-T03 and under magnification found that this sample has the most resemblance to the normal human blood without losing the polyethylene composite properties, bringing us the closest to our desired result. Further tests and analysis shows that the sample has passed all compatability tests and matching sequences, confirming that the new sample has fulfilled all the qualities needed for a synthetic blood, bringing the human body compatability percentage to 92%. I am glad to affirm that this new sample is ready for the project’s next stage— experimentations on actual human bodies.

DR J WARNEY 11. 06. 2310

32


E.A.S.E

KEY PROCEDURE IN TRANSFUSION HUMAN BLOOD PULSE FUSION

EQUIPMENT CHECKED AND TESTED BY MS HELENA

HC 20. 06. 2310

VACUUM TRANSFUSIONER

33


EQUIPMENT CHECK-02

PULSE ENTERS BLOODSTREAM THROUGH OSMOSIS

PULSE

X-RBC

34


E.A.S.E

1 2 . 07. 2 3 1 0

SUBJECTS PROFILE The subjects involved have all agreed to partake in this experiment for the benefit of scientific evolution and the development of mankind.

TEST CODE: P101

SCOUTED AND APPROVED BY DR SOO.

PROCEDURE:

Subjects will go through blood transfusion of PULSE at 50cc. Thereafter they will be injected with daily dosages.

M01

35

N01


SUBJECTS PROFILE

SUBJECT M01:

FEMALE, 27 S T A T U S : H E A LT H Y , ABLE-BODIED H E I G H T: 1 6 0 C M W E I G H T: 5 2 KG BLOOD TYPE: O NO ALLERGIES NO HISTORY OF MEDICAL ILLNESS

ORIGINS: DISTRICT X

DNA STRUCTURE:

36


E.A.S.E

10. 08. 2310

SUBJECT M01 MONITOR: Day 01 since subject was injected with PULSE batch L436.

S TAT U S : H E A LT H Y , N O R M A L

BLOOD LEVELS

MAIN COMPONENTS: IRON PULSE WAT E R GLUCOSE SODIUM

30% Glucose

37

17% Sodium

47% Iron

58.1% PULSE

23% Water


M01 MONITOR

H E A R T R AT E : ECG HH(32)

+0.5 X S L-1 M M

BPM

70

BP

111/60 X 32.1 MAX-

REMARKS: S ub j ec t’s vita ls a re w e l l an d sh e i s f u n c t i o n i n g a s p er norma l. Subje ct wil l co n t i n u e d o sage of P UL S E L436. Keep s ubje ct in th e w hi t e ro o m w h i l e b e i n g m o nit ored .

DR H.SOO 10. 08. 2310

38


E.A.S.E

! A L E RT: SUBJECT M01

12. 08. 2310

S TAT U S : CRITICAL Day 03 since subject was injected with PULSE batch L436.

REPORT Subject‘s heart rate plummeted below 50 at 15.03.

H E A R T R AT E M O N I TO R AT 1 5 . 3 5 ECG HH(32)

+0.5 X S L-1 M M

39

BPM

40


M01-MONITOR

U P D AT E D I N T I M E W I T H THE SUBJECT’S TRACKER

16.00: Subject rushed for treatment and diagnosis.

16.10: Subject transfused with normal human blood.

16.30: Subject’s heart rate drops to 10.

1 7. 0 0 : Resuscitation efforts has been carried out for 30 mins.

PRONOUNCED DEAD T I M E O F D E AT H : 1 7. 2 0

40


PROJECT HALTED_ _ _



E.A.S .E .


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