WO2001035943A2 - Dextrose and insulin fluid formulation for intravenous infusion - Google Patents

Dextrose and insulin fluid formulation for intravenous infusion Download PDF

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Publication number
WO2001035943A2
WO2001035943A2 PCT/IN2000/000110 IN0000110W WO0135943A2 WO 2001035943 A2 WO2001035943 A2 WO 2001035943A2 IN 0000110 W IN0000110 W IN 0000110W WO 0135943 A2 WO0135943 A2 WO 0135943A2
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Prior art keywords
dextrose
insulin
vitamins
fluids
solutions
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PCT/IN2000/000110
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French (fr)
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WO2001035943A3 (en
Inventor
Hanamaraddi T. Gangal
Parag H. Gangal
Madhumati H. Gangal
Original Assignee
Gangal Hanamaraddi T
Gangal Parag H
Gangal Madhumati H
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by Gangal Hanamaraddi T, Gangal Parag H, Gangal Madhumati H filed Critical Gangal Hanamaraddi T
Priority to AU30489/01A priority Critical patent/AU779798C/en
Priority to JP2001537936A priority patent/JP2003514014A/en
Priority to EP00990877A priority patent/EP1231907A2/en
Publication of WO2001035943A2 publication Critical patent/WO2001035943A2/en
Publication of WO2001035943A3 publication Critical patent/WO2001035943A3/en

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    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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    • A61K31/07Retinol compounds, e.g. vitamin A
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    • A61K31/13Amines
    • A61K31/14Quaternary ammonium compounds, e.g. edrophonium, choline
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    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
    • A61K31/198Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
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    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
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    • A61K31/726Glycosaminoglycans, i.e. mucopolysaccharides
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Definitions

  • Ringers lactate solutions etc. All these have been used, as basic fluids when patient needed administration of therapeutic fluids and other ingredients. In certain special circumstances, fluids like
  • the body is unable to utilise, the energy substrate and electrolytes available, in view of high levels of catacholamines, along with qualitative and quantitative deficiency of insulin, and disturbed hormonal levels.
  • the fluids needed are broadly categorised for use to suit the various situations. They are to be in packing of 500 ml for calculations .
  • the following abbreviations are used to denote the fluid and their possible place of use.
  • G - Gangal N - Non diabetic, D - Diabetic, E - Electrolytes, H - Heparin, V - Vitamins, I - Insulin, where supplemental Potassium is added they are marked as K.
  • Dext - Dextrose Dextrose.
  • A.E Actual electrolytes to replace the Extra cellular electrolytes
  • A.M Actual electrolytes needed in Maintenance solutions as are presently available, to be taken as 500 ml packing for values of their contents.
  • the fluids needed to treat patients who are said to be non-diabetic, as are known to day, are called GN 1 containing the ingredients as stated in the abbreviated text form in the columns
  • the GD 9 solutions are supplemented with Electrolytes and Vitamins to gain GD 14 - EV solutions.
  • the GD 9 group of fluids is supplemented with Heparin and Vitamins. They provide GD 15 - H V group of solutions.
  • the GD 9 combination fluids are supplemented with Electrolytes, Heparin and Vitamins. These fluids form the GD 16 - EHV. Group of solutions
  • the tables below provide information about A.E, the Actual electrolytes in Extra cellular replacement and A.M, Actual electrolytes in Maintenance solutions as are available.
  • the values expressed in the table against each item is the actual content of the ingredients in 100 ml of each fluids as are in use today.
  • Oil Soluble Vitamins A, D, E, are made water soluble to be used here.
  • the formulations consist of the following and other ingredients mentioned in the above clarifications and in the text.
  • Water is the main and the essential natural component of the body, and is also the main vehicle / media through which the body's circulation is maintained. This makes it possible the essentials of life and function are made available from the body to the cell level and receives back the wastes from the cell level to the organ to be eliminated out of the body. It helps to mentain physiological state in and around the body, congenial to sustain normal life.
  • the volume of the water needed by the body varies with the functional level, the problems faced and the environment. Accordingly the volume of fluid needed to be infused, to balance the need and the output and also to maintain an effective circulation, are required into consideration to asses.
  • Dextrose A major source of energy out of all other essential energy substrates. A must for living and sustaining life.
  • Dextrose in the form of 5% as an isotonic solution has been the main stay of intravenous infusion in all forms of conditions where infusion forms the treatment as well as a resuscitative measure. In states of stress, shock, and critical conditions, this isotonic solution is now understood to have hypotonic solution effect.
  • This type of fluids are likely to cause enormous harmful effects.
  • the fluids we use in hypertonic form enable us to provide needed higher calories along with insulin, and also avoid effects of hypotonic solutions.
  • it forms the main source of energy to be supplemented by amino acids, and emulsified fat solutions. This helps to meet the needs of essential amino acids, and also fats; along with it enables to prevent the bad and rebound effects of prolonged use of carbohydrates alone.
  • Na Sodium chloride forms a major and a main electrolyte. It is also called the second pump to maintain the circulation.
  • Nacl is an isotonic solution, commonly used as such or in combination with Dextrose solutions. It is one of the main electrolyte, the body needs. It is mainly an extra cellular electrolyte with a small intracellular component, having a reciprocal gradient relation with K ion responding to any effective agents. The intake and output needs to be balanced. The body contains a large amount, nearing around 5000 mEq of Na, with an average need of, 80 - 100, mEq / Day. This is mostly lost in the urine. In the normal individual, on one hand there is a large reserve, on the other hand there is an excellent mechanism to conserve it by normal functioning kidney. This can result in bringing urinary loss of Na to near zero, in the absence of intake ofNa. Still large fluctuations do occur with resultant serious problems. Hence it needs to be managed properly to retain homeostasis
  • Ca Calcium similarly forms a major cation component of the body, having role to play in homeostasis, membrane potentials, inter cellular junctions and cell functions.
  • Calcium forms around 2% of the bodyweight. Ninety nine % of it is in the form of bone. Part of it is constantly changing to contribute to the extra-cellular component. This is under the influence of simple ion exchange. Paratharmone, Vit D, Corticosteroids cause disturbances in Calcium content.
  • any variations in the extra-cellular component affect the homeostasis. This in turn results in deranged cellular functions.
  • Average Indian diet may contain as low as 0.2 Gms as against the daily need of 0.5 to 0.6 gm on an average. The needs are higher in later terms of pregnancy and lactation, thus needing up to around 1 gram of Calcium a day.
  • Intracellular Ca regulates cell metabolism, it's function and inter junction permeability.
  • Ca is an important component of the cell membrane and competes with Na. Raised Ca, in blood increases the threshold for contraction and low Ca leads to tetany.
  • Ca also plays role in coagulation of blood, coupling mechanism between excitation and contraction of muscles, and secretary mechanism of Insulin.
  • K Potassium mainly an intracellular electrolyte having a significant role to play in cell membrane potentials and cell functions.
  • Potassium chloride KC1 solution is available for intravenous use, needs to be diluted considerably to use. Normally there is about 3500 mEq of Potassium in the body, of which 98%is intracellular and hardly 2% is in extra-cellular compartment. This small part of the Potassium plays a major role in the functioning of the smooth, skeletal, and cardiac muscles. As a result any variations that occur in its level can certainly cause considerable problems.
  • electrolytes As are included in the A.E, extra cellular electrolyte replacement component and A.M, electrolyte maintenance replacement component solutions are also essential to the body's function and are required to be maintained in balance.
  • Insulin Insulin is an essential hormone required in the process of metabolism of carbohydrates, proteins, and fats. Involving almost all organs in the body. It is now fairly well established, in clinical states needing intravenous infusions, there is qualitative and quantitative deficiency of insulin.
  • Heparin It is a naturally occurring substance, not occurring in blood to a measurable extent, prevents blood coagulation. It plays significant role in cases of trauma induced on any account. Blood coagulation is essentially a series of enzymatic reactions involving a number of plasma proteins. Many of these are present only in traces. Within an intact healthy circulatory system these enzymes, for the most part, are in an inactive form, when the blood is shed on wettable surfaces, a series of auto catalytic enzymatic reaction is initiated, this is a process of more complex and confused in results, interpretations, and opinions.
  • Vitamins Fat and water-soluble vitamins are organic compounds, forming as components or cofactors for enzymes concerned with metabolism of carbohydrates, fats, and proteins.
  • Vitamin A -Daily dose of around 10,000 to 20,000 I.U in the form of made as water soluble could be essential to maintain the integrity of the epithelial cells, synthesis of glucocortcoids, cholesterol, and for somatic growth, upper respiratory tract epithelium.
  • Vitamin Bi It is mainly concerned with Carbohydrate metabolism. IV / IM administration of large doses may cause anaphylactic shock and interfere with action of other B vitamins.
  • B 3 - Nicotinic acid is required in Protein metabolism, necessary in respiration Be - Indirectly affects carbohydrate metabolism, directly the catacholamines, gamma-amino butyric acid, etc., B 7 - is involved in fundamental biological reactions.
  • B ⁇ is necessary in maintenance of function of the nervous system and conduction mechanism.
  • C - Concerned with cellular respiration / oxidation-reduction reactions, and formation of collagen, intercellular matrix development of cartilage, wound healing, carbohydrate metabolism.
  • Vitamin D - Facilitates interdepartmental metabolism between vitamins, and maintains Ca. homeostasis. It is quite important in the acute conditions, like mobilisation of insulin, coupling mechanism of excitation and contraction mechanism of muscles. These have some relevance to diabetes normal organ function and essential hypertension.
  • E - Alpha Tocopheryl Acetate is said to be essential to maintain integrity and stability of biological membranes, normal structure and function of the nervous system and is mostly used on an empirical base. It is known to be antioxidant.
  • Choline Chloride is akin to B group of Vitamins but synthesised in the human body. It plays an important role as a structural component of tissues and in biological methilation reactions. It is a precursor of acetylcholine, and some hormones. Its biogenesis is universal in nature. It helps to spare amino acids in protein synthesis.
  • DL - Methionine is sulphur containing aminoacid and inseparable dietary component. Methionine has lipotropic action, and is considered as useful adjutant of treatment of liver diseases. It enhances synthesis of glutathione, necessary for detoxification of toxic metabolites of paracetamol. Average needs are around 200 to 500 mgm.
  • Inosital - occurs in nearly all plant, and animal cell, suggesting it to be an essential cell constituent. It is found to be a constituent of an amylase enzyme system. To a certain extent it is synthesised by the intestinal flora. It possesses weak lipotropic activity prevents fatty liver. It could be beneficial in diabetic neuropathy.

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Abstract

Intravenous infusion formulations comprising dextrose, insulin, electrolytes and optionally heparin and vitamins.

Description

DEXTROSE AND INSULIN FLUID FORMULATION FOR INTRAVENOUS INFUSION.
BY DR.H.T.GANGAL, HOSUR, HUBLI. 580021. KARNATAKA. INDIA.
Patients receive intravenous fluids in the form of nutrients minerals vitamins antibiotics and other life saving drugs in a number of clinical conditions. It is also reliable and effective means of providing them with predictable effects and minimum of inconvenience.
This may be the only means of treatment feasible in many occasions as a measure of resuscitative procedure to revive the patients from critically ill state to a state of survival and back to normal life.
The presently available fluids are inadequate in all aspect except the water content of the need of the patient. They are hypotonic in effect even though they are isotonic when used in critical conditions. The author has been feeling, the needs of the patients under such circumstances by the presently infused fluids are hardly met. Thus putting the patient in a state of disadvantage to face the situation and to recover back to normal.
Preamble
With the development of science the desires and expectations of the patients keep on improving in terms of better results, at less cost, effort, and loss of working time, in previously treatable cases. And revival and prolongation of life when earlier they were not possible. Much has been achieved in these directions in medical science. As part of the treatment even today the intravenous infusions consist mainly water dextrose electrolytes. Subsequently the same route has been utilised for administration of antibiotics, proteins and lipid solutions along with many other soluble materials needed in particular instances.
The commonly used solutions are in packing of 500 ml in the form of
1. 5% Dextrose
2. 0.9% NaCl solutions
3. Ringers lactate solutions etc. All these have been used, as basic fluids when patient needed administration of therapeutic fluids and other ingredients. In certain special circumstances, fluids like
1. 10% Dextrose
2. 10% Dextrose in normal saline (0.9%)
3. 20-25% Dextrose
4. Dialysis fluids
5. Blood and blood components
6. Low Molecular Dextrans
7. Mannitol
8. Bulk form antibiotics and
9. Many other drugs have been used today.
Now, it appears evident that, we have been providing insufficient and inadequate calories; from limited sources of these needed calories by way of energy substrates. So also the electrolytes, vitamins and other needed elements. This late awareness of inadequate knowledge on the needs of the treatment of stress, shock, and critical conditions has resulted in many centres to put up added attention and efforts to study and evaluate the effects. This effort has lead to more specific and allied in formations to be available, stressing the need to restore homeostasis towards normal, by restoring tissue perfusion and acid base balance towards normal. This will enable to improve the condition, to revive and restore normalcy, as has been stressed by the investigator. The presently available fluids are
1. Unable to meet the calorie need of the patient. These needed calories require to originate from dextrose, aminoacids, and fats.
2. Unable to meet the electrolytes required by the patient, in terms of variety and quantity,
3. The body is unable to utilise, the energy substrate and electrolytes available, in view of high levels of catacholamines, along with qualitative and quantitative deficiency of insulin, and disturbed hormonal levels.
All these effects lead to a state of catabolism. Their consequential effects on the body are aptly described as a state of autocannibalism. We need to stop or prevent this from happening or continuing. This emphasises, the infusions to provide the needs of the body in terms of, calorie, electrolytes, vitamins and other essentials to enable and utilise to treat, improve, revive and restore normalcy. Prophylactic measures on this line of approach in expected situations like major operative procedures enable one to minimise the risks of the procedure considerably.
The fluids needed are broadly categorised for use to suit the various situations. They are to be in packing of 500 ml for calculations .The following abbreviations are used to denote the fluid and their possible place of use. G - Gangal, N - Non diabetic, D - Diabetic, E - Electrolytes, H - Heparin, V - Vitamins, I - Insulin, where supplemental Potassium is added they are marked as K. PL - Plain / Soluble bovine insulin or Potentially equivalent Human insulin preferred. Dext - Dextrose. A.E - Actual electrolytes to replace the Extra cellular electrolytes, A.M - Actual electrolytes needed in Maintenance solutions as are presently available, to be taken as 500 ml packing for values of their contents. The fluids needed to treat patients who are said to be non-diabetic, as are known to day, are called GN 1 containing the ingredients as stated in the abbreviated text form in the columns
Sr.no GN 1
1 10%Dext + 0.9%Nacl + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 16 IU PL Insulin
IK 10%Dext + 0.9%Nacl + 0.6875gm Cal Glu + 20 mEq Kcl (1.50 gm) + 16 IU PL Insulin
2 10%Dext in A.E Sol + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 16 IU PL Insulin
3 10%Dert in A.M.Sol + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 16 IU PL Insulin
4 15%Dext + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 24 IU PL Insulin
5 20%Dext + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 32 IU PL Insulin
5K 20%Dext + 0.6875gm Cal Glu + 20 mEq Kcl (1.50 gm) + 32 IU PL Insulin
There could be / are occasions where electrolyte requirements could be higher. In such situation we need to provide higher doses in the form GN 2 - E Group of solutions
Figure imgf000004_0001
There could be / are occasions where Heparin may be required and can be added to GN 1 Group of Solutions. These fluids thus formed could be called as GN3 - H Group of Solutions
Figure imgf000004_0002
There could be / are occasions where Vitamins may be required and can be added to GN 1 Group of Solutions. These fluids thus formed could be called as GN 4 - V Group of Solutions
Sr.no GN 4 - V
10%Dext + 0.9%Nacl + 0.6875gm Cal Glu + 10 mEq Kcl (0.75 gm) + 16 IU PI Insulin Vitamins A, D, E, B-comp,C, CC, DL-M, I
Figure imgf000005_0001
There could be / are occasions where electrolyte requirements could be higher along with the need of Heparin. In such situation we need to provide these doses in the form of GN 5 - EH group of solutions.
Figure imgf000005_0002
There could be / are occasions where requirements could be the need of additional electrolytes and also Vitamin along with GN 1 Solutions. In such situation we need to provide these doses in the form of GN 6 - EV group of solutions O 01/35943
Figure imgf000006_0001
There could be / are occasions where requirements could be the need of, Heparin and also Vitamins along with GN 1 Solutions. In such situation we need to provide these doses in the form of GN 7- HV group of solutions
Figure imgf000006_0002
There could be / are occasions where requirements could be the need of higher amounts of Electrolytes, Heparin and also Vitamins along with GN 1 Solutions. In such situation we need to provide these doses in the form of GN 8 — EHV group of solutions
Figure imgf000007_0001
The use of GN 1 fluids in treating manifest diabetic cases, the need of insulin will be definitely more. Hence additional quantity of insulin is added to this group of solutions called GD 9.
Figure imgf000007_0002
There could be/are occasions where electrolyte requirements could be higher than in GD 9 solutions In such situation we need to provide higher doses to provide tenth group solutions called GD 10.- E
Sr. no GD 10 - E
Figure imgf000008_0001
There could be / are occasions where Heparin may be required and can be added to GD 9 Group of Solutions. These fluids thus formed could be called as GD 11 - H Group of Solutions
Figure imgf000008_0002
There could be / are occasions where Vitamins may be required and can be added to GD 9 Group of Solutions. These fluids thus formed could be called as GD 12 - V Group of Solutions
Sr.no GD 12 - V
10%Dex + 0.9%Nacl + 0.6875 gm Cal Glu + 10 mEq Kcl (0.75 gm) + 20 IU PL Insulin Vitamins A, D, E, B-comp,C, CC, DL-M, I
IK 10%Dex + 0.9%Nacl + 0.6875 gm Cal Glu + 20 mEq Kcl (1.50 gm) + 20 IU PL Insulin Vitamins A, D, E, B-comp,C, CC, DL-M, I
10%Dex in A.E Sol + 0.6875 gm Cal Glu + 10 mEq Kcl (0.75 gm) + 20 IU PL Insulin
Figure imgf000009_0001
There could be / are occasions where electrolyte requirements could be higher along with the need of Heparin. In such situation we need to provide these doses in the form of GD 13 - EH group of solutions
Figure imgf000009_0002
The GD 9 solutions are supplemented with Electrolytes and Vitamins to gain GD 14 - EV solutions.
Sr . no GD 14 - E V
10%Dext + 0.9%Nacl + 1.032 gm Cal Glu + 15 mEq Kcl (1.125 gm) + 20 IU PL Insulin Vitamins A, D, E, B-comp, C, CC, DL-M, I
IK 10%Dext + 0.9%Nacl + 1.032 gm Cal Glu + 20 mEq Kcl (1.500 gm) + 20 IU PL Insulin Vitamins A, D, E, B-comp, C, CC, DL-M, I
Figure imgf000010_0001
The GD 9 group of fluids is supplemented with Heparin and Vitamins. They provide GD 15 - H V group of solutions.
Figure imgf000010_0002
The GD 9 combination fluids are supplemented with Electrolytes, Heparin and Vitamins. These fluids form the GD 16 - EHV. Group of solutions
Sr . no GD 16 - E HV
10%Dext + 0.9%Nacl + 1.032 gmCal Glu + 15 mEq Kcl (1.125 gm) + 20 IU PL Insulin Vitamins A, D, E, B-comp,C, CC, DL-M, I 1000 IU Heparin
IK 10%Dext + 0.9%NacI + 1.032 gmCal Glu + 20 mEq Kcl (1.500 gm) + 20 IU PL Insulin
Figure imgf000011_0001
Clarification information
The tables below provide information about A.E, the Actual electrolytes in Extra cellular replacement and A.M, Actual electrolytes in Maintenance solutions as are available. The values expressed in the table against each item is the actual content of the ingredients in 100 ml of each fluids as are in use today.
Figure imgf000011_0002
Bicarbonate Precursor - Osmolarity (A-E Solutions) Approx 570 Calculated Osmolarity (A-M Solutions) Approx 400 Concentration of Electrolytes in (mEq / L)
Figure imgf000011_0003
Figure imgf000012_0001
The Vitamins added per 500 ml of fluids.
Figure imgf000012_0002
Oil Soluble Vitamins A, D, E, are made water soluble to be used here.
With these improved formulations, it has been possible to meet the largely needed requirements under various types of critical clinical conditions, as can be rationalised to day.
One should appreciate; these formulations may be able to meet the needed requirements. They will enable us to standardise the approach, and give scope in future a better way to improve further the formulations. Thus will enabling us to gain still further occasion to improve the formulations to attain better results within scope of the appended claims in formulations. We may also gain better and larger scope of their use in various other conditions.
The formulations consist of the following and other ingredients mentioned in the above clarifications and in the text.
1. Water: Water is the main and the essential natural component of the body, and is also the main vehicle / media through which the body's circulation is maintained. This makes it possible the essentials of life and function are made available from the body to the cell level and receives back the wastes from the cell level to the organ to be eliminated out of the body. It helps to mentain physiological state in and around the body, congenial to sustain normal life. The volume of the water needed by the body varies with the functional level, the problems faced and the environment. Accordingly the volume of fluid needed to be infused, to balance the need and the output and also to maintain an effective circulation, are required into consideration to asses.
2. Dextrose: A major source of energy out of all other essential energy substrates. A must for living and sustaining life.
Dextrose in the form of 5% as an isotonic solution has been the main stay of intravenous infusion in all forms of conditions where infusion forms the treatment as well as a resuscitative measure. In states of stress, shock, and critical conditions, this isotonic solution is now understood to have hypotonic solution effect. This type of fluids, are likely to cause enormous harmful effects. Where as the fluids we use in hypertonic form enable us to provide needed higher calories along with insulin, and also avoid effects of hypotonic solutions. Normally it forms the main source of energy to be supplemented by amino acids, and emulsified fat solutions. This helps to meet the needs of essential amino acids, and also fats; along with it enables to prevent the bad and rebound effects of prolonged use of carbohydrates alone. This results in accumulation of acidic components and triggering of catacholamine response, indeed an unwanted response at an odd occasion to result in further effects to an already critical condition. Here, 10%, 15%, 20%, are used to provide higher amount of dextrose along with insulin, electrolytes, vitamins, and Heparin to meet the high levels of metabolism. This is likely to avoid auto cannibalism and its consequent outcome of survival.
3. Na: Sodium chloride forms a major and a main electrolyte. It is also called the second pump to maintain the circulation.
Sodium Chloride: 0.9% Nacl is an isotonic solution, commonly used as such or in combination with Dextrose solutions. It is one of the main electrolyte, the body needs. It is mainly an extra cellular electrolyte with a small intracellular component, having a reciprocal gradient relation with K ion responding to any effective agents. The intake and output needs to be balanced. The body contains a large amount, nearing around 5000 mEq of Na, with an average need of, 80 - 100, mEq / Day. This is mostly lost in the urine. In the normal individual, on one hand there is a large reserve, on the other hand there is an excellent mechanism to conserve it by normal functioning kidney. This can result in bringing urinary loss of Na to near zero, in the absence of intake ofNa. Still large fluctuations do occur with resultant serious problems. Hence it needs to be managed properly to retain homeostasis
4. Ca: Calcium similarly forms a major cation component of the body, having role to play in homeostasis, membrane potentials, inter cellular junctions and cell functions.
Calcium: Calcium forms around 2% of the bodyweight. Ninety nine % of it is in the form of bone. Part of it is constantly changing to contribute to the extra-cellular component. This is under the influence of simple ion exchange. Paratharmone, Vit D, Corticosteroids cause disturbances in Calcium content.
Any variations in the extra-cellular component affect the homeostasis. This in turn results in deranged cellular functions. Average Indian diet may contain as low as 0.2 Gms as against the daily need of 0.5 to 0.6 gm on an average. The needs are higher in later terms of pregnancy and lactation, thus needing up to around 1 gram of Calcium a day. Intracellular Ca regulates cell metabolism, it's function and inter junction permeability.
With normally functioning kidneys, 99% of the Ca gets reabsorbed from the tubules. Urinary Ca excretion increases with hypercalcaemia of any cause, metabolic acidosis and use of cortisones.
Ca is an important component of the cell membrane and competes with Na. Raised Ca, in blood increases the threshold for contraction and low Ca leads to tetany.
Ca also plays role in coagulation of blood, coupling mechanism between excitation and contraction of muscles, and secretary mechanism of Insulin.
5. K: Potassium mainly an intracellular electrolyte having a significant role to play in cell membrane potentials and cell functions.
Potassium chloride: KC1 solution is available for intravenous use, needs to be diluted considerably to use. Normally there is about 3500 mEq of Potassium in the body, of which 98%is intracellular and hardly 2% is in extra-cellular compartment. This small part of the Potassium plays a major role in the functioning of the smooth, skeletal, and cardiac muscles. As a result any variations that occur in its level can certainly cause considerable problems.
Seventy-five percent of the Potassium is found in the skeletal muscles. Normally on an average the body needs around 50 to 80 mEq of Potassium per day. The main route of loss is through normally functioning kidney. The minimum that is lost through urine could be 20 mEq even in the absence of
Potassium intake.
In view of the high quantity of Potassium is in intracellular compartment any injury to the organs is bound to increase the extra-cellular Potassium. It is to a certain extent dependent on the level of
Sodium, other hormones and diuretics. Its movements / transfer is related to metabolism.
There are occasions where intracellular Potassium deficiency may be present although the plasma level is normal; such situations need careful evaluation than casual look.
6. Other electrolytes: As are included in the A.E, extra cellular electrolyte replacement component and A.M, electrolyte maintenance replacement component solutions are also essential to the body's function and are required to be maintained in balance.
All these have been used in clinical application.
7. Insulin: Insulin is an essential hormone required in the process of metabolism of carbohydrates, proteins, and fats. Involving almost all organs in the body. It is now fairly well established, in clinical states needing intravenous infusions, there is qualitative and quantitative deficiency of insulin.
8. Heparin: It is a naturally occurring substance, not occurring in blood to a measurable extent, prevents blood coagulation. It plays significant role in cases of trauma induced on any account. Blood coagulation is essentially a series of enzymatic reactions involving a number of plasma proteins. Many of these are present only in traces. Within an intact healthy circulatory system these enzymes, for the most part, are in an inactive form, when the blood is shed on wettable surfaces, a series of auto catalytic enzymatic reaction is initiated, this is a process of more complex and confused in results, interpretations, and opinions.
Heparin when added as a therapeutic agent, it acts at a number of sites along the chain of reaction. Its probable initial, action is to prevent the development of thromboplastin activity. Heparin has immediate action on the coagulation system. It is a naturally occurring sulfonated polysaccharide with strong anticoagulant action. It is rapidly inactivated and removed from the circulation. It is difficult to maintain therapeutic level in the blood while avoiding the danger from bleeding. Here it is used to prevent likely initiation of early thromboembolic phenomenon.
In the present situation medical science is not as exact as mathematics and it may not be so forever. Life science is so complex, and every effort, to understand, evaluate, or treat, involves, time, money, risk and need of invasive procedures, with added risks. 9. Vitamins: Fat and water-soluble vitamins are organic compounds, forming as components or cofactors for enzymes concerned with metabolism of carbohydrates, fats, and proteins.
Most of the vitamins are acquired from dietary sources. Very few to a small extent are synthesised in the body.
B. Group vitamins act, as essential co-enzymes required as intermediary in the metabolism. Dietary vitamins need to be converted to its co-enzyme form in order to be useful. It is also noted these vitamins are interdependent on their metabolism and utilisation. In the absence of sources of supply, use of various drugs affecting their metabolism, that too under circumstances of raised metabolic state, there, does occur an occasion to provide these needed Vitamins in the form of intravenous administration.
These Vitamins are classified, as Fat Soluble Vitamins, A D.E.K are stored in the body.
Water Soluble Vitamins, B Group & C are not stored and any excess is rapidly excreted in the urine. They are not toxic. And tend not to cause interaction with drugs.
This likely Vitamin deficiency occurring during total parenteral nutrition, are attended by providing as follows.
Vitamin A: -Daily dose of around 10,000 to 20,000 I.U in the form of made as water soluble could be essential to maintain the integrity of the epithelial cells, synthesis of glucocortcoids, cholesterol, and for somatic growth, upper respiratory tract epithelium.
Vitamin Bi - It is mainly concerned with Carbohydrate metabolism. IV / IM administration of large doses may cause anaphylactic shock and interfere with action of other B vitamins. B3 - Nicotinic acid is required in Protein metabolism, necessary in respiration Be - Indirectly affects carbohydrate metabolism, directly the catacholamines, gamma-amino butyric acid, etc., B7 - is involved in fundamental biological reactions.
Bπ . is necessary in maintenance of function of the nervous system and conduction mechanism. C: - Concerned with cellular respiration / oxidation-reduction reactions, and formation of collagen, intercellular matrix development of cartilage, wound healing, carbohydrate metabolism. Vitamin D: - Facilitates interdepartmental metabolism between vitamins, and maintains Ca. homeostasis. It is quite important in the acute conditions, like mobilisation of insulin, coupling mechanism of excitation and contraction mechanism of muscles. These have some relevance to diabetes normal organ function and essential hypertension.
E: - Alpha Tocopheryl Acetate is said to be essential to maintain integrity and stability of biological membranes, normal structure and function of the nervous system and is mostly used on an empirical base. It is known to be antioxidant.
Choline Chloride is akin to B group of Vitamins but synthesised in the human body. It plays an important role as a structural component of tissues and in biological methilation reactions. It is a precursor of acetylcholine, and some hormones. Its biogenesis is universal in nature. It helps to spare amino acids in protein synthesis.
It prevents fatty infiltration of liver, a hypertropic agent; average estimated consumption appears to be around 500 to 900 mgm/a day.
DL - Methionine: - is sulphur containing aminoacid and inseparable dietary component. Methionine has lipotropic action, and is considered as useful adjutant of treatment of liver diseases. It enhances synthesis of glutathione, necessary for detoxification of toxic metabolites of paracetamol. Average needs are around 200 to 500 mgm.
Inosital: - occurs in nearly all plant, and animal cell, suggesting it to be an essential cell constituent. It is found to be a constituent of an amylase enzyme system. To a certain extent it is synthesised by the intestinal flora. It possesses weak lipotropic activity prevents fatty liver. It could be beneficial in diabetic neuropathy.
Stress, trauma, shock, critical conditions, sepsis, surgery increase the catabolic rate. This increased catabolism is a self-destructive response to the above stated illnesses. It is termed as auto cannibalism needing everyone's attention to prevent it occurring.
The developments in medical sciences appear to have been based mostly on the outcome of interested individuals efforts. There has been no systematic developmental effort to study life science, as it stands smaller priority, in the Government and personal levels. Hence allocation of funds in comparison with defence, industry etc is very meagre. In such circumstances the evaluations are difficult. Presently adopted methods of treatment are largely based on the individual knowledge, and capability to evaluate the condition he is handling. Thus giving large scope for variations and the resultant outcomes. On the background of the experience in the experimental surgery in developing open heart surgery and handling critically ill patients, major trauma patients, the concept adopted by me and resultant comparatively better outcomes led me to continue the work and peruse to gain further information on the line. I continued to try the concept in conditions where the senior colleagues could not expect any hope (with appreciable good results), convinced me, the approach stands better scope in the present situation. With more and more information now available, the scope of use of my concept has enlarged and the results have proved its worthiness to be pursued. It needs fair variations with the fundamental concept remaining to be the backbone in all its variant approach in different clinical pictures.
I feel stress, trauma, shock critical conditions; surgery infections cause state of disturbed neuro- hormonal response resulting in changed hormonal catacholamine levels, homeostatic conditions, altered level of defence mechanism and metabolism. All needs to be attended, to provide proper physiological response to restore normalcy and recovery. This needs the approach to be well balanced, gradual, predictable and reasonable, to gain near natural normal life, without the need of prolonged therapy assisted sustenance of life.
1) I also feel every individual is potentially diabetic, hypertensive more so under states of stress and allied situations is now corroborated by quite a few.
2) There is a raised metabolism under states of stress & critical condition leading to auto cannibalism, a worst situation leading to multiple organ dysfunction syndromes.
As a preventive measure to minimise such occurrences, I use these fluids, in
1 ) Stress - Primary Hypertension Angina pectoris.
2) Shock, a) Multiple traumatic injuries. b) Perforative peritonitis c) Pancreatitis d) Major operative procedures e) Major vascular surgeries.
Like thrombo-end arterectomies
Meso-caval anatomises in portal hypertension etc.
3) Cirrhosis of liver
4) Scorpion strings, Snake bites
5) Bacterial resistant infections - Septic shock
6) In conditions a) Coronary Artery diseases b) Myocardial Infarcts c) Following Cardie- Vascular Surgeries
7) Adult Respiratory distress Syndromes. / Multi-organ Dysfunction Syndrome 8) In the treatment of Cancer
9) Poly - Cystic Kidney
10) Alzheimer's disease & many other clinical conditions associated with critical situations.
1 1)
These fluids possibly by their concurrent use in conditions like HIV and Australian Antigen Virus infection rabies, and tetanus may provide better results by restoring the cell and organ environment, to a near normal level, and assist the defence mechanism of the body they have beneficial effects on the cell membrane.

Claims

We Claim
A. Dextrose and Insulin fluid formulation for intravenous infusion treatment comprises a formulation having synergistic interaction.
B. It contains
1. Water, the main media, 500-ml. 2. Dextrose 10% to 20%
3. Insulin 0.32 to 0.40. 1.U, /Gm of Dextrose 4. Sodium Chloride (NaCl) 0 to 4.5Gms
5. Calcium Gluconate 0.6875 to 1.375Gms 6. Potassium Chloride (KC1) 0 to 1.5 Gms
7. Sodium Acetate 0 to 3.2 Gms 8. Sodium Citrate 0 to 375 mgm
9. Calcium Chloride 0 to 260 mgm 10. Magnesium chloride 0 to 155 mgm
1 1. Sodium Meta-Bisulphite 0 to 105 mgm 12. Dibasic Potassium Phosphate 0 to 0.65 Gms
C. Vitamins I.P.
13. Vitamin A 0 to 4000 I U 14. Thiamine Hydrochloride I.P. 0 to 50 mg
15. Pyridoxine Hydrochloride I.P. 0 to 6 mg 16. Riboflavin Sodium Phosphate 0 to 6
17. Nicotinamide I.P. 0 to 50 mg 18. D.Pantothenol I.P. 0 to 10 mg
19. Vitamin B12 I.P 0 to 15 meg 20. Ascorbic acid IP 0 to 200 mg
21. Cholecalciferol I.p. 0 to 300 IU 22 Alpha Tocoferil Acetate I.P. 0 to 2 mg
23. Choline chloride 0 to 5 mg 24. Di-methionine 0 to 5 mg
25. Inositol 0 to 3 mg
D. Heparin 0 to 1000 IU
The above claims A, B, C and D enable me to claim further that these fluids are effective in treating the conditions stated above.
The above formulations have proved effective all along for use on immediate use of their formulation. In case there is going to be problem of stability of the formulation, they will necessarily be put in combination (separate) packages suitable for mixing immediately prior to its use. ABSTRACT
DEXTROSE AND INSULIN FLUID FORMULATION FOR INTRAVENOUS INFUSION. BY DR.H.T.GANGAL, HOSUR, HUBLI. 580021. KARNATAKA. INDIA.
Patients receive intravenous fluids in the form of, fluid, media, nutrients minerals vitamins antibiotics and other life saving drugs in a number of clinical conditions. It is also reliable and effective means of providing them predictable effects with πύiumum of inconvenience.
This may be the only means of treatment feasible on many occasions as a measure of resuscitative procedure to revive the patients from critically ill state to a state of survival and back to normal life.
The presently available fluids are inadequate in all aspect except the water content of the need of the patient. They are hypotonic in effect even though they are isotonic when used in critical conditions. The author has been feeling, the needs of the patients under such circumstances by the presently infused fluids are hardly met. Thus putting the patient in a state of disadvantage to face the situation and to recover back to normal. With the development of science the desires and expectations of the patients keep on improving in terms of better results, at less cost, effort and loss of working time, in previously treatable cases. And revival and prolongation of life when earlier they were not possible. Much has been achieved in these directions in medical science. As part of the treatment even today the intravenous infusions consist mainly water dextrose electrolytes. Subsequently the same route has been utilized for administration of antibiotics, Proteins and lipid solutions along with many other soluble materials needed in particular instances.
Sequence listing part of description
1. Introduction of Dextrose And Insulin Fluid Formulation for Intravenous Infusion.
2. Preamble .
3. Background of abbreviations.
4. Formulations in tabulations.
5. Clarification information on A.E., and A.M., Solutions.
6. Osmolarity.
7. Concentration of Electrolytes.
8. Vitamins per 500 ml of fluids.
9. Ingredients like Water, Dextrose.
10. Ingredients like electrolytes.
11. Ingredients like Insulin, and Heparin.
12. Ingredients like vitamins and other precursors.
13. Field of application.
14. Scope of its application in future.
PCT/IN2000/000110 1999-11-15 2000-11-10 Dextrose and insulin fluid formulation for intravenous infusion WO2001035943A2 (en)

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JP2004002429A (en) * 2002-05-29 2004-01-08 Insignion Holdings Ltd Composition and therapeutic application of the same
WO2007072147A2 (en) * 2005-12-19 2007-06-28 Ernst, Johanna, Catarina Composition for diagnosing and treating circulatory system diseases
US9901623B2 (en) 2015-08-27 2018-02-27 Eli Lilly And Company Rapid-acting insulin compositions
US10646551B2 (en) 2012-11-13 2020-05-12 Adocia Rapid-acting insulin formulation comprising a substituted anionic compound
US11123406B2 (en) 2014-12-16 2021-09-21 Eli Lilly And Company Rapid-acting insulin compositions
US11207384B2 (en) 2017-06-01 2021-12-28 Eli Lilly And Company Rapid-acting insulin compositions

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2546286C2 (en) * 2013-06-07 2015-04-10 Федеральное государственное бюджетное научное учреждение "Всероссийский научно-исследовательский институт крахмалопродуктов" Pharmaceutical substance and method of obtaining thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1982003773A1 (en) * 1981-04-27 1982-11-11 Baxter Travenol Lab Dialysis solution containing glucose,amino acids & insulin
WO1991018610A1 (en) * 1990-05-28 1991-12-12 Olle Ljungqvist Medical Ab New use of glucose and a new solution of glucose
WO1995005833A1 (en) * 1993-08-24 1995-03-02 Albert Fay Hill Pharmaceutical composition for immunoenhancement therapy

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1982003773A1 (en) * 1981-04-27 1982-11-11 Baxter Travenol Lab Dialysis solution containing glucose,amino acids & insulin
WO1991018610A1 (en) * 1990-05-28 1991-12-12 Olle Ljungqvist Medical Ab New use of glucose and a new solution of glucose
WO1995005833A1 (en) * 1993-08-24 1995-03-02 Albert Fay Hill Pharmaceutical composition for immunoenhancement therapy

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
DATABASE EMBASE [Online] ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL; HASLAUER F. ET AL: "[The effect of an infusion of glucose- insulin -potassium and of heparin on the concentration of plasma free fatty acids and blood glucose]. DIE WIRKUNG EINER INFUSION VON GLUKOSE- INSULIN -KALIUM UND VON HEPARIN AUF DIE KONZENTRATION DER FREIEN FETTSAUREN DES PLASMAS UND DER BLUTGLUKOSE." retrieved from STN Database accession no. 83253537 XP002171110 & WIENER KLINISCHE WOCHENSCHRIFT, (1983) 95/17 (618-621). CODEN: WKWOAO, *
DATABASE EMBASE [Online] ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL; MARCUARD S.P. ET AL: "Availability of insulin from total parenteral nutrition solutions." retrieved from STN Database accession no. 90165762 XP002171111 & JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, (1990) 14/3 (262-264). , *
DATABASE MEDLINE [Online] US NATIONAL LIBRARY OF MEDICINE (NLM), BETHESDA, MD, US; WEBER S S ET AL: "Availability of insulin from parenteral nutrient solutions." retrieved from STN Database accession no. 77179246 XP002171112 & AMERICAN JOURNAL OF HOSPITAL PHARMACY, (1977 APR) 34 (4) 353-7. , *
SHIZGAL H M ET AL: "INSULIN AND EFFICACY OF TOTAL PARENTERAL NUTRITION" AMERICAN JOURNAL OF CLINICAL NUTRITION,BETHESDA,MD,US, vol. 50, 1989, pages 1355-1363, XP000569039 ISSN: 0002-9165 *

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004002429A (en) * 2002-05-29 2004-01-08 Insignion Holdings Ltd Composition and therapeutic application of the same
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WO2007072147A3 (en) * 2005-12-19 2007-11-01 Ernst Johanna Catarina Composition for diagnosing and treating circulatory system diseases
US10646551B2 (en) 2012-11-13 2020-05-12 Adocia Rapid-acting insulin formulation comprising a substituted anionic compound
US10881716B2 (en) 2012-11-13 2021-01-05 Adocia Rapid-acting insulin formulation comprising a substituted anionic compound
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US11207384B2 (en) 2017-06-01 2021-12-28 Eli Lilly And Company Rapid-acting insulin compositions

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