Low molecular weight polyethylene glycol drug conjugates having improved drug biological activity

Abstract

Provided are polyethylene glycol drug conjugates of general formula (I), (II) or (III) and pharmaceutical compositions and a use thereof. The conjugates are formed by combining low molecular weight polyethylene glycol with 2-4 drug molecules. The conjugates can interact with receptor dimers or polymers, thereby improving the in vivo distribution of the drug, changing the oil and water distribution coefficient, enhancing the pharmacological activity, reducing the blood-brain barrier permeability of the drug, and improving the bioavailability of the drug.

Claims

1. A drug-polyethylene glycol-drug conjugate of formula (I), the conjugate being formed by combining low molecular weight polyethylene glycol with two drug molecules,
TA-X-PEG-X′-TA′   (I) Wherein: PEG is a polyethylene glycol residue having the following structure, ##STR00017## n is an integer of 0-25; X, X′ are linking groups which may be identical or different, selected from a group consisting of ##STR00018## i is an integer of 0-10; TA, TA′ are target compounds that may be identical or different, selected from a group consisting sumatriptan, dorzolamide, irinotecan, camptothecin, dasatinib, paclitaxel, docetaxel, Dccyclovirobuxinum D, diethyl stilbestrol, estradiol, prazosin, terazosin, metoclopramide, ursodesoxycholic acid, rapamycin, scopolamine, and procaine.

2. The conjugate according to claim 1, wherein n is an integer of 0-10.

3. The conjugate according to claim 1, wherein i=2, and X, same as X′, is —(CH.sub.2CH.sub.2)O—.

4. The conjugate according to claim 1, wherein TA is the same as TA′ and selected from a group consisting of sumatriptan, dorzolamide and dasatinib.

5. A drug composition comprising the conjugate according to claim 1 and a pharmaceutically acceptable carrier or excipient.

6. A drug composition comprising the conjugate according to claim 1 and a pharmaceutically acceptable salt, wherein the pharmaceutically acceptable salt is selected from a group consisting of hydrochloride, hydrobromate, sulphate, nitrate, phosphate, citrate, tartrate, fumarate, maleate, lactate, benzene sulfonate, pantothenate, ascorbate or combinations thereof.

7. The drug composition according to claim 5, and wherein the drug composition is in the form of tablet, suppository, pill, soft and hard gelatin capsule, powder, solution, suspension or aerosol.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a view showing a 3-D structure of a heterodimer of Mu-delta opioid peptide receptor.

DETAILED DESCRIPTION OF THE INVENTION

(2) Polyethylene glycol units are used to indicate low polyethylene glycol. Generally, the number of the included polyethylene glycol units is used to indicate low polyethylene glycol, the number of polyethylene glycol units is an integer of 0-20, preferably an integer of 3-10.

(3) The polyethylene glycol in the present invention includes derivatives and analogues of polyethylene glycol and may be substituted by one of the following hydrophilic polymers, which is selected from a group consisting of polyethylene glycol, polyglutamic acid, polyaspartic acid, polypropylene glycol, polyvinyl alcohol, polypropylene morpholine, polyoxazolone and copolymers thereof.

(4) The conjugate of the present invention may be administered in a form of a pure compound or a suitable drug composition, in any acceptable administration manner, or used for a reagent with similar use. Therefore, the employed administration manner may be selected from oral administration, intranasal administration, non-intestinal administration, local administration, percutaneous administration or rectum administration, administration takes a form of solid, semisolid or liquid medicament, e.g., tablet, suppository, pill, soft and hard gelatin capsule, powder, solution, suspension or aerosol, and preferably employs a unit dosage enabling simple administration with an accurate dosage. The composition may include a conventional drug carrier or excipient and the conjugate of the present invention as an active component (one or more kinds), and additionally may comprise other medicaments, carriers, adjuvants and the like.

(5) Usually, according to the desired administration manner, the pharmaceutically acceptable composition will include about 1 to 99 weight percent conjugate of the present invention, and 99-1 weight percent suitable medical excipient. Preferably, the composition includes about 5-75 weight percent conjugate of the present invention, with the balance being a suitable medical excipient.

(6) According to the drug composition that may be administered in form of a liquid, for example, the conjugate (about 0.5-about 20%) of the present invention and selectively-existing medicinal adjuvants are solved and dispersed in a carrier by a solving and dispersing means to form a solution or suspension, wherein examples of the carrier is water, saline, glucose hydrate, glycerol, ethanol or the like.

(7) If necessary, the drug composition of the present invention may further include a small amount of assistant substance such as a wetting agent or emulsifier, pH buffering agent, and antioxidant, for example, citric acid, sorbitan monolaurate, trithanolamine oleate, butylated hydroxytoluene.

(8) The following examples are used to illustrate the present invention, but not used to limit the present invention.

(9) Sumatriptan used in the examples are provided by Jiangsu Ocean Biological Engineering Co., Ltd, dasatinib is provided by Nanjing Ange Pharmaceutical and Chemical Co., Ltd, metoxyethoxymethyl chloride (MEMCL) is provided by Alfa Aesar, paratoluensulfonyl chloride is purposed from Shandong Yilong Industrial Co., Ltd, sodium hydride is purchased from TCI (Shanghia) Chemical Industry Development Co., Ltd., and H(OCH.sub.2CH.sub.2).sub.4—OH, H(OCH.sub.2CH.sub.2).sub.6—OH and H(OCH.sub.2CH.sub.2).sub.12—OH are purchased from Jiaxing Bomei Biotechnology Co., Ltd. Other reagents used in examples of the present invention all are reagents available in the market.

Examples

Example 1 Synthesis of Double End-Substituted Hexaethyleneglycol-Sumatriptan (SMQT-01)

(10) ##STR00007##

(11) Hexaethyleneglycol (1) (2.5 ml, 10 mmol) is dissolved in 50 mL dichloromethane, triethylamine (4.17 ml, 10 mmol) is added, methanesulfonyl chloride (1.72 mL, 22 mmol) is dripped in, and reaction continues 16 hours at a room temperature under nitrogen gas protection. 1.2 ml methanol is added and stirred 15 minutes, filtering is performed to remove solid to concentrate to obtain 3.85 g product (2), with a yield rate 99%, which is directly used for next reaction.

(12) Hexaethyleneglycol disulfonate (2) (3.85 g, 10 mmol) and 13.3 g tetrabutyl ammonium bromide are dissolved in acetonitrile 50 mL, and stirred and react 16 hours under nitrogen gas protection. Solvent is evaporated out, acetic ether and water are added for extraction, extract is dried by using anhydrous sodium sulfate, concentrates and goes through column separation to obtain 2.85 g product (3), with a yield rate 80%. .sup.1H-NMR (CDCl.sub.3): 3.82 (t, 4H), 3.67 (s, 16H), 3.48 (t, 4H).

(13) Sumatriptan (236 mg, 0.8 mmol) is dissolved in 2 mL dry DMF, 60% NaH (32 mg, 0.8 mmol) is added, stirred and react 15 minutes, then the compound (3) (163.2 mg, 0.4 mmol) is added, and reaction is performed overnight under nitrogen gas protection. Water is added to the above reaction liquid to quench the reaction, extraction is performed three times by using acetic ether, an organic phase is dried by using anhydrous sodium sulfate, concentrate goes through column separation to obtain 240 mg product, with a yield rate 61%. .sup.1H-NMR (CDCl.sub.3): 2.34 (s, 12H), 2.63 (t, 4H), 2.77 (s, 6H), 2.93 (t, 4H), 3.13 (t, 4H), 3.44 (t, 4H), 3.51 (s, 16H), 4.34 (s, 4H), 6.98 (s, 2H), 7.14 (d, 2H), 7.26 (d, 2H), 7.57 (s, 2H), 8.91 (s, 2H).

Example 2 Synthesis of Double End-Substituted Pentaethyleneglycol-Sumatriptan (SMQT-02)

(14) Pentaethyleneglycol (2.38 g, 10 mmol) is dissolved in 50 mL dichloromethane, triethylamine (4.16 ml, 10 mmol) is added, methanesulfonyl chloride (1.77 mL, 22 mmol) is dripped in, and reaction continues 16 hours at a room temperature under nitrogen gas protection. 1.2 ml methanol is added and stirred 15 minutes, filtering is performed to remove solid to concentrate to obtain 3.94 g product, with a yield rate 99%, which is directly used for next reaction.

(15) Pentaethyleneglycol disulfonate (3.94 g, 10 mmol) and 13.3 g tetrabutyl ammonium bromide are dissolved in acetonitrile 50 mL, and stirred and react 16 hours under nitrogen gas protection. Solvent is evaporated out, acetic ether and water are added for extraction, extract is dried by using anhydrous sodium sulfate, concentrates and goes through column separation to obtain 2.73 g product, with a yield rate 75%. .sup.1H-NMR (CDCl.sub.3): 3.49 (t, 4H), 3.69 (s, 12H), 3.84 (t, 4H).

(16) Sumatriptan (236 mg, 0.8 mmol) is dissolved in 2 mL dry DMF, 60% NaH (32 mg, 0.8 mmol) is added, stirred and react 15 minutes, triethylene glycol 2-bromoethyl (145.6 mg, 0.4 mmol) is added, and reaction is performed overnight under nitrogen gas protection. Water is added to the above reaction liquid to quench the reaction, extraction is performed three times by using acetic ether, an organic phase is dried by using anhydrous sodium sulfate, concentrate goes through column separation to obtain 184 mg product, with a yield rate 58%. .sup.1H-NMR (CDCl.sub.3): 2.34 (s, 12H), 2.70 (t, 4H), 2.72 (s, 6H), 2.94 (t, 4H), 3.06 (t, 4H), 3.40 (t, 4H), 3.49 (s, 12H), 4.35 (s, 4H), 6.98 (s, 2H), 7.11 (d, 2H), 7.23 (d, 2H), 7.60 (s, 2H), 8.91 (s, 2H).

Example 3 Synthesis of Double End-Substituted Triethylene Glycol-Sumatriptan (SMQT-03)

(17) Triethyleneglycol (2.67 ml, 20 mmol) is dissolved in 50 mL dichloromethane, triethylamine (8.33 mL, 20 mmol) is added, methanesulfonyl chloride (3.44 mL, 44 mmol) is dripped in, and reaction continues 16 hours at a room temperature under nitrogen gas protection. 1.2 ml methanol is added and stirred 15 minutes, filtering is performed to remove solid to concentrate to obtain 6.12 g product, with a yield rate 99%, which is directly used for next reaction.

(18) Triethyleneglycol disulfonate (4.12 g, 13.46 mmol) and 17.3 g tetrabutyl ammonium bromide are dissolved in acetonitrile 50 mL, and stirred and react at 50° C. 16 hours under nitrogen gas protection. Solvent is evaporated out, acetic ether and water are added for extraction, extract is dried by using anhydrous sodium sulfate, concentrates and goes through column separation to obtain 2.84 g product, with a yield rate 77%. .sup.1H-NMR (CDCl.sub.3): 3.49 (t, 4H), 3.70 (s, 4H), 3.84 (t, 4H).

(19) Sumatriptan (236 mg, 0.8 mmol) is dissolved in 2 mL dry DMF, 60% NaH (32 mg, 0.8 mmol) is added, stirred and react 15 minutes, then ethylene glycol 2-bromoethyl (109.6 mg, 0.4 mmol) is added, and reaction is performed overnight under nitrogen gas protection. Water is added to the above reaction liquid to quench the reaction, extraction is performed three times by using acetic ether, an organic phase is dried by using anhydrous sodium sulfate, concentrate goes through column separation to obtain a product, with a yield rate 61%. .sup.1H-NMR (CDCl.sub.3): 2.35 (s, 12H), 2.66 (t, 4H), 2.72 (s, 6H), 2.94 (t, 4H), 3.07 (t, 4H), 3.40 (t, 4H), 3.47 (s, 4H), 4.34 (s, 4H), 6.98 (s, 2H), 7.12 (d, 2H), 7.23 (d, 2H), 7.60 (s, 2H), 8.91 (s, 2H).

Example 4 Synthesis of Double End-Substituted Tetraethylene Glycol-Dasatinib (DSTN-42)

(20) ##STR00008##

(21) 19.1 g paratoluensulfonyl chloride and 40 mL pyridine are added in 250 mL three-neck flask, and cooled to 0° C. 9.7 g HO-PEG(n=4)-OH is mixed uniformly with 20 mL pyridine, and then dripped in the three-neck flash, and the temperature is controlled between 0 and 10° C. Stirring and reaction is continued at this temperature for two hours. TLC monitors that the reaction is complete. 300 mL cold water and 60 mL concentrated hydrochloric acid are added in the reaction liquid and slowly stirred for half an hour, then the reaction liquid is transferred into a 500 mL separating funnel, acetic ether is added to extract twice (300 mL+200 mL). The organic layers are merged and washed by water to neutrality, dried by anhydrous sodium sulfate for two hours. A rotary evaporator evaporates out solvent to obtain 21.4 g viscous liquid, which will be directly used for next reaction.

(22) 487 g dasatinib and 166 mg potassium carbonate are added into a 100 mL three-neck flask filled with 20 mL acetonitrile, and stirred at a room temperature for two hours. 10 mL acetonitrile solution in which 258 mg TsO-PEG(n=4)-OTs is dissolved is added to the reaction flask, and reflex reacts overnight. TLC monitors that the reaction is complete. Column separation is carried out to obtain 308 mg white solid with a yield rate 54.5%. m/z [MH].sup.+1133. .sup.1H-NMR (DMSO-d6): 2.23 (s, 6H), 2.49 (s, 6H), 2.51 (m, 8H), 3.53 (m, 32H), 6.04 (s, 2H), 7.27 (m, 4H), 7.40 (m, 2H), 8.22 (s, 2H), 9.88 (s, 2H), 11.48 (s, 2H).

Example 5 Synthesis of Methoxyl Pentaethylene Glycol-Dasatinib (DSTN-51)

(23) ##STR00009##

(24) 9.6 g paratoluensulfonyl chloride and 40 mL pyridine are added in 250 mL three-neck flask, and cooled to 0° C. 12.6 g mPEG(n=5)-OH is mixed uniformly with 20 mL pyridine, and then dripped in the three-neck flash, and the temperature is controlled between 0 and 10° C. Stirring and reaction is continued at this temperature for two hours. TLC monitors that the reaction is complete. 300 mL cold water and 60 mL concentrated hydrochloric acid are added in the reaction liquid and slowly stirred for half an hour, then the reaction liquid is transferred into a 1000 mL separating funnel, acetic ether is added to extract twice (300 mL+200 mL). The organic layers are merged and washed by water to neutrality, dried by anhydrous sodium sulfate for two hours. A rotary evaporator evaporates out solvent to obtain 21.5 g viscous liquid, which will be directly used for next reaction.

(25) 253 g dasatinib and 128 mg potassium carbonate are added into a 100 mL three-neck flask filled with 20 mL acetonitrile, and stirred at a room temperature for two hours. 10 mL acetonitrile solution in which 205 mg mPEG(n=5)OTs is dissolved is added to the reaction flask, and reflex reacts overnight. TLC monitors that the reaction is complete. Column separation is carried out to obtain 205 mg white solid with a yield rate 56.8%. m/z [MH].sup.+722. .sup.1H-NMR (DMSO-d6): 2.24 (s, 3H), 2.43 (s, 3H), 2.51 (m, 8H), 3.22 (s, 3H), 3.61 (m, 20H), 6.05 (s, 1H), 7.27 (m, 2H), 7.41 (m, 1H), 8.22 (s, 1H), 9.88 (s, 1H), 11.48 (s, 1H).

Example 6 Synthesis of Double End Hexaethylene Glycol-Dasatinib (DSTN-62)

(26) ##STR00010##

(27) 19.1 g paratoluensulfonyl chloride and 40 mL pyridine are added in 500 mL three-neck flask, and cooled to 0° C. 14.1 g HO-PEG(n=6)-OH is mixed uniformly with 20 mL pyridine, and then dripped in the three-neck flash, and the temperature is controlled between 0 and 10° C. Stirring and reaction is continued at this temperature for two hours. TLC monitors that the reaction is complete. 300 mL cold water and 60 mL concentrated hydrochloric acid are added in the reaction liquid and slowly stirred for half an hour, then the reaction liquid is transferred into a 1000 mL separating funnel, acetic ether is added to extract twice (300 mL+200 mL). The organic layers are merged and washed by water to neutrality, dried by anhydrous sodium sulfate for two hours. A rotary evaporator evaporates out solvent to obtain 28.7 g viscous liquid, which will be directly used for next reaction.

(28) 506 g dasatinib is dissolved in 6 ml N,N-dimethylformamide, 160 mg NaH is added, and stirred at a room temperature for one hour. 302 mg TsO-PEG(n=6)-Ots is added for reaction at a room temperature for 20 hours. TLC monitors that the reaction is complete. Column separation is carried out to obtain 316 mg white solid with a yield rate 51.8%. m/z [MH].sup.+1221. .sup.1H-NMR (DMSO-d6): 2.19 (s, 6H), 2.28 (s, 6H), 2.49 (m, 8H), 3.61 (m, 40H), 6.04 (s, 2H), 7.20 (m, 4H), 7.41 (m, 2H), 8.18 (s, 2H), 9.87 (s, 2H), 11.46 (s, 2H).

Example 7 Single End Substituted Pentaethyleneglycol-Dorzolamide (DZA-01)

(29) ##STR00011##

(30) Nonaethyleneglycol monomethyl (4.28 g, 10 mmol) is dissolved in 50 mL dichloromethane, triethylamine (4.16 ml, 10 mmol) is added, methanesulfonyl chloride (0.9 mL, 11 mmol) is dripped in, and reaction continues 16 hours at a room temperature under nitrogen gas protection. 1.2 ml methanol is added and stirred 15 minutes, filtering is performed to remove solid to concentrate to obtain a product, which is directly used for next reaction.

(31) The above obtained product and 6.80 g tetrabutyl ammonium bromide are dissolved in 50 mL acetonitrile, and stirred and react at 50° C. for 16 hours under nitrogen gas protection. Solvent is evaporated out, acetic ether and water are added for extraction, extract is dried by using anhydrous sodium sulfate, concentrates and goes through column separation to obtain 3.38 g product, with a yield rate 68%.

(32) Dorzolamide (324 mg, 1 mmol) is dissolved in 2 mL dry DMF, 60% NaH (40 mg, 1 mmol) is added, stirred and react 15 minutes, an intermediate (491 mg, 1 mmol) is added, and reaction is performed overnight under nitrogen gas protection. Water is added to the above reaction liquid to quench the reaction, extraction is performed three times by using acetic ether, an organic phase is dried by using anhydrous sodium sulfate, concentrate goes through column separation to obtain 352 mg product, with a yield rate 48%. m/z [MH].sup.+735.

Example 8 Double End Substituted Hexaethyleneglycol-Dorzolamide (DZA-02)

(33) ##STR00012##

(34) Reference is made to Example 6 for the syntheses method. m/z [MH]+895.

Example 9 Double End Substituted Odecylethyleneglycol-Dorzolamide (DZA-03)

(35) H(OCH.sub.2CH.sub.2).sub.12—OH is used to substitute hexaethyleneglycol. Reference is made to Example 6 for the syntheses method. m/z [MH].sup.+1159.

Example 10 Three-Branch Ethyleneglycol-Dorzolamide Conjugate (DAZ-04)

(36) Regarding syntheses of three-branch ethyleneglycol (H), please refer to US2006/0047167.

(37) Reference is made to Example 6 for the syntheses method. m/z [MH].sup.+1157.

(38) ##STR00013##

Example 11 Three-Branch Ethyleneglycol-Dorzolamide Conjugate (DAZ-05)

(39) ##STR00014##

(40) Regarding syntheses of the compound L, please refer to J. Org. Chem. 2006, 71, 9884-9886.

(41) Reference is made to Example 6 for the syntheses method. m/z [MH].sup.+1818.

Example 12 Four-Branch Ethyleneglycol-Dorzolamide Conjugate (DAZ-06)

(42) Regarding syntheses of the four-branch ethyleneglycol, please refer to Bulletin of Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 38; nb. 10; (1989); p. 2207.

(43) ##STR00015##

(44) Reference is made to Example 6 for the syntheses method. m/z [MH].sup.+1538.

Example 13 Four-Branch Ethyleneglycol-Dorzolamide Conjugate (DAZ-07)

(45) Regarding syntheses of the compound R, please refer to J. Org. Chem. 2006, 71, 9884-9886.

(46) ##STR00016##

(47) Reference is made to Example 6 for the syntheses method. m/z [MH].sup.+2490.

Example 14 Inhibition of Dasatinib Series Compounds for Cell Proliferation and IC50 Measurement

(48) Research Purpose

(49) Detection is performed for the function of three kinds of drugs for proliferation of tumor cells K562, KU812, SUP-B15, and PC-3, to determine its 50% inhibition centration (IC50).

(50) Research Scheme

(51) Cells are cultured under a complete culture medium; when cells are attached to the wall, drug of different concentrations is added in each tumor cell line for treatment, and a positive control, a blank control and a solvent control are set. Cells are incubated for 72 hours and then CTG method is used for detection.

(52) TABLE-US-00001 TABLE 1 IC50 (μM) results Serial IC50 (μM) number Cell line DSTN-51 DSTN-42 DSTN-62 1 PC-3 83.12 — — 2 SUP-B15 0.17 0.05 0.06 3 K562 0.00222 0.00050 0.00034 4 KU812 0.00050 0.00079 0.00049 Notes: “—” indicates that IC50 value cannot be calculated

(53) TABLE-US-00002 TABLE 2 Maximum inhibition rate Serial Maximum inhibition rate (%) number Cell line DSTN-51 DSTN-42 DSTN-62 1 PC-3 56.67 30.97 29.74 2 SUP-B15 91.39 93.36 81.47 3 K562 79.04 80.34 81.76 4 KU812 96.47 96.91 96.00

Example 15 Transmembrance Transport Action of Polyethylene Glycol-Modified Series Compounds

(54) Caco-2 is an epithelial cell of human colon cancer, it may differentiate and grow on its own into epithelial cell monolayer having a structure and function similar to small intestine and represented with an active transportor and partial metabolic enzyme, and is a good model for evaluating in vitro membrane permeability. According to a standard culture procedure of the Caco-2 cell, a cell monolayer is prepared on a Transwell culture insert, a culture hole having a transmembrane resistance greater than 300 Ω.Math.cm.sup.2 is selected to perform a transmembrane experiment, and positive quality control drugs atenolol (which can penetrate the membrane difficulty) and methyltestosterone (which can penetrate the membrane easily) are selected in parallel to perform necessary quality control for the experimental system.

(55) 1. Unidirectional Transport Experiment

(56) 400 μL quality control drug (atenolol or methyltestosterone) or a drug to be tested is added respectively into holes of an upper pond of the culture insert, 500 μL Hank's liquid pre-incubated at 37° C. is added in a lower pond, incubation is performed in CO.sub.2 incubator for 90 min, the solution of the lower pond is collected, quantitatively processed and measured to calculate its appearance penetration coefficient (Papp):
Papp=(dQ/dt)/(A.Math.C.sub.0)

(57) Wherein dQ is an accumulated penetration amount of a drug receiving pond with a measure unit μmol; dt is incubation time with a measure unit min; A is a diffusion area with a measure unit cm.sup.2; C.sub.0 is an initial administration concentration of an administrating pond with a measure unit μmol.Math.L.sup.−1; Papp has a measure unit cm/s.

(58) A universal standard for evaluating Caco-2 cell transmembrane transport penetration is that Papp>100×10.sup.−6 indicates a compound which penetrates the membrane easily; 100×10.sup.−6>Papp>10×10.sup.−6 indicates a compound which penetrates the membrane at a medium level; Papp<10×10.sup.−6 indicates a compound that penetrates the membrane difficulty.

(59) 2. Bidirectional Transport Experiment

(60) An evaluation objective of the bidirectional transport is to preliminary observe that the transmembrane transport of the object to be tested has active transport procedure mediated by an efflux transporter. Positive quality-control drug digoxin and a drug to be tested are added respectively in holes of the upper pond or lower pond of the culture insert, Hank's liquid pre-incubated at 37° C. is added in an opposite pond, incubation is performed in CO.sub.2 incubator for 90 min, the solution of the opposite pond is collected, quantitatively processed and measured to calculate its appearance penetration coefficient (PappA-B and PappB-A) according to the above formula and a ratio of the two; when the ratio is >2, it is prompted that the transmembrane transport of the compound might involve active transport mediated by an efflux transporter.

(61) The experimental results of transmembrane transport are shown as follows:

(62) TABLE-US-00003 Papp(B.fwdarw.A)/ Compound Papp(*10.sup.−6)A.fwdarw.B Papp(*10.sup.−6)B.fwdarw.A Papp(A.fwdarw.B) SMQT-01 10.55 ± 0.36  15.50 ± 0.06 1.47 SMQT-02 9.87 ± 0.03 14.52 ± 0.12 1.47 SMQT-03 6.25 ± 0.51 11.06 ± 0.21 1.77 DSTN-51 8.55 ± 2.29 23.91 ± 1.24 2.80 DSTN-42 4.57 ± 0.87 11.43 ± 0.72 2.50 DSTN-62 6.44 ± 0.11 15.01 ± 0.59 2.33 DZA-01 11.54 ± 0.36  15.50 ± 0.06 1.34 DZA-02 12.32 ± 0.34  25.50 ± 1.21 2.07 DZA-03 8.96 ± 0.35 23.67 ± 0.45 2.64 DZA-04 6.76 ± 0.24 11.53 ± 0.58 1.71 DZA-05 6.85 ± 0.46 23.87 ± 0.57 3.48 DZA-06 8.86 ± 0.51 18.12 ± 0.32 2.05 DZA-07 6.50 ± 0.06 25.88 ± 0.53 3.98

Example 16 Blood-Brain Barrier Permeability

(63) The drug in plasma is enabled to reach a steady state by using a rat model in a manner of injection at an even speed, to see a ratio value (Kp value) of a drug concentration in the plasma and a drug concentration in brain tissue upon the steady state, to represent a distribution capability of the drug in the brain tissue. It is characterized by reliable data, direct provision of blood/brain distribution ratio value of the compound, and saving of animals and dosage.

(64) Sumatriptan Series:

(65) Research results show that the blood-brain barrier permeability of the three compounds is all lower than sumatriptan, wherein the blood-brain barrier permeability of SMQT-01 compound is 1/50 of sumatriptan, the blood-brain barrier permeability of SMQT-02 compound is 1/37 of sumatriptan, and the blood-brain barrier permeability of SMQT-03 compound is 1/13 of sumatriptan.

(66) Dasatinib Series:

(67) Research results show that the blood-brain barrier permeability of the three compounds is all lower than dasatinib, wherein the blood-brain barrier permeability of DSTN-42 compound is 1/18 of dasatinib, the blood-brain barrier permeability of DSTN-51 compound is 1/23 of dasatinib, and the blood-brain barrier permeability of DSTN-62 compound is 1/33 of dasatinib.

(68) Dorzolamide Series

(69) Research results show that the blood-brain barrier permeability of seven compounds is all lower than dorzolamide, wherein the blood-brain barrier permeability of DZA-01 compound is 1/55 of dorzolamide, the blood-brain barrier permeability of DZA-02 compound is 1/34 of dorzolamide, the blood-brain barrier permeability of DZA-03 compound is 1/65 of dorzolamide, the blood-brain barrier permeability of DZA-04 compound is 1/12 of dorzolamide, the blood-brain barrier permeability of DZA-05 compound is 1/28 of dorzolamide, the blood-brain barrier permeability of DZA-06 compound is ⅛ of dorzolamide, and the blood-brain barrier permeability of DZA-07 compound is 1/27 of dorzolamide.

Example 17 Experiment on Absolute Bioavailability of Polyethylene Glycol-Sumatriptan Conjugate

(70) Animal: male SD rat

(71) Groups of the experiment: intravenous injection group and oral administration group, four rats being provided for each rat

(72) Dosage: determined by a preliminary experiment

(73) Administration manner: tail intravenous injection, intragastric administration

(74) Blood sampling point: determined by a preliminary experiment

(75) Data processing: an area under a curve is calculated for intravenous injection and oral administration by using a trapezoidal method, and a bioavailability is calculated by using the following formula:

(76) $F=\frac{{\mathrm{AUC}}_{p.o.}\times {\mathrm{Dose}}_{i.v.}}{{\mathrm{AUC}}_{i.v.}\times {\mathrm{Dose}}_{p.o.}}\times 100\%$

(77) Research results show that absolute bioavailability of SMQT-01 compound is 17%, absolute bioavailability of SMQT-02 compound is 23%, and absolute bioavailability of SMQT-03 compound is 25%.